The toothpaste
Science

Why 5% potassium nitrate: the dose the trials used, and what nobody has tested.

Five per cent is the concentration of potassium nitrate the published toothpaste trials used, from the placebo-controlled trials of the 1990s to a manufacturer-funded four-arm randomised trial published in 2026: it is the tested dose, not the top of a strength ladder, and no trial has ever compared two concentrations of potassium nitrate in a toothpaste110. The only randomised comparison of two potassium nitrate concentrations anywhere used bioadhesive gels instead of paste, ran for fourteen days in 45 patients, and its authors called the result preliminary11. S3 Sensitivity Science™ declares 5% potassium nitrate on its ingredient list, one of three rows in the September 2026 category review whose published ingredient information gives a potassium nitrate level at all, and one of the only two of those three on sale in the UK, the third being a US listing.

What was checked25 peer-reviewed studies, product information as published by each brand, and guidance from the Oral Health Foundation and the NHS

Key points
  • Every potassium nitrate toothpaste in the published trial literature carries 5%: the 12-week randomised trial that reported complete relief of symptoms in 67% of the treated group against 6% on placebo used it, and so did the manufacturer-funded randomised trial published in 2026110.
  • Nobody has run the trial that would settle how much potassium nitrate a paste needs: five PubMed searches run for this page found no dose-ranging toothpaste trial, and the one direct comparison of two concentrations used a gel and separated on one measure of three11.
  • What travels with the 5% varies from paste to paste, and a scoping review counted potassium compounds in 68 of the 368 formulations tested in the trial literature, a literature that divides between two main fluoride salts and two families of abrasive16; where an eight-week randomised trial funded by a manufacturer changed only that, the paste carrying 5% potassium nitrate with a copolymer came out ahead of the paste carrying the same 5% without it from week two10.
  • Twelve rows of the September 2026 category review list potassium nitrate in their published ingredients. Three give a level, and all three give the same one: 5%.
  • Five per cent is the concentration the published studies used, and S3 is formulated at it, which is a statement about matching the evidence and not about beating anything.

What does "strongest" mean on a sensitivity toothpaste, and can you read it off the pack?

You cannot, on most packs, because the number that would answer the question is not printed. A UK toothpaste has to publish its ingredient list, and most adult packs give their fluoride in parts per million, but the level of a desensitising active appears only if the brand decides to print it. In the September 2026 category review, twelve rows list potassium nitrate somewhere in their published ingredient information. Nine give no figure for it.

This page compares ingredients and stated actions only, not clinical performance, based on what each brand states about its own formula. Prices and formulations may change; always check the pack. Every row below resolves to a public listing through its CR id, and each was read on the date shown.

Product, as the listing spells itPotassium nitrate level declaredFluoride, as publishedWater baseWhere it was readRowRead
Sensodyne Pronamel Daily Protection5% w/wsodium fluoride 0.315% w/w, 1450 ppmyesBootsCR-0042026-09-09
Sensodyne Daily Care Originalnot statedsodium fluoride 0.315% w/w, 1450 ppmyesBootsCR-0062026-09-09
Sensodyne Complete Protection+ Originalnot statedsodium fluoride 0.315% w/w, 1450 ppmyesBootsCR-0072026-09-09
Colgate Sensitive Instant Relief Multi Protectionnot statedsodium fluoride, 1450 ppmyesBootsCR-0112026-09-09
Colgate Sensitive with Sensifoam Multi Protectionnot statedsodium fluoride, 1450 ppmyesBootsCR-0122026-09-09
Colgate Max White Clinical Sensitive Protectnot statedsodium monofluorophosphate, 1450 ppmnoBootsCR-0142026-09-09
Boots Everyday Sensitive Toothpastenot statedsodium fluoride 0.32% w/w, 1450 ppmyesBootsCR-0192026-09-09
Superdrug Procare Sensitive Toothpastenot statedsodium fluoride, no ppm figure on the pageyesSuperdrugCR-0572026-09-09
Waken Sensitive Care Toothpastenot statedsodium fluoride, 1450 ppmyesbrand siteCR-0332026-09-09
Zendium Sensitivenot statedsodium fluoride, 1450 ppmyesAmazon UK listing; the brand site blocks automated readersCR-0442026-09-09
TheraBreath Sensitive Toothpaste5%sodium fluoride 0.24%, no ppm figureyesUS site; UK availability not establishedCR-0492026-09-09
S3 Daily Sensitive Toothpaste5%sodium monofluorophosphate, 1450 ppmyesbrand siteCR-0282026-09-09

Two things follow from the table, and only two. The first is that "strongest" cannot be read off this shelf, because for nine of the twelve there is no number to compare. The second is that where a number is given it is always the same number. Not one row anywhere in the scan declares a potassium nitrate level other than 5%. The strength ladder people are looking for does not exist on the shelf, and the rest of this page is about why it does not exist in the literature either.

A shelf-level version of this question, which takes every desensitising active and not just this one, is in the guide to reading strength off a UK sensitivity pack, and the aisle-by-aisle read of the two big chemists is in sensitive toothpaste at Boots and Superdrug. This page stays with one ingredient and one number.

Where does the 5% come from?

From the trials, and from nowhere else. Potassium nitrate has sat in desensitising toothpastes since the 1970s, and placebo-controlled trials of it date from the 1990s. Those trials were run at 5%, and every trial since has stayed there1234. In a twelve-week double-blind trial of 36 adults, a 5% paste improved cold-air, tactile and self-rated scores at four, eight and twelve weeks, and 67% of the treated group reported complete relief of symptoms against 6% on placebo1. A twelve-week randomised trial of 67 adults found significant improvement against a matching placebo at six and twelve weeks2. A multicentre randomised trial reported significant reductions against placebo on every index at four weeks4. An eight-week randomised trial of 48 adults tested the same 5% with 1500 ppm sodium monofluorophosphate in a precipitated calcium carbonate base and found significant improvement at four and eight weeks3.

That is the origin of the figure, and it is worth being exact about what it is: a formulation choice that was made once, tested, and then copied. The concentration was not arrived at by testing several and keeping the best.

One number in circulation looks like a second rung on the ladder and is not. Three per cent is a mouthwash concentration, used in rinses tested on their own against fluoride rinses and against no active, and a rinse is a different product with a different contact time. It is not a weaker toothpaste, and it does not give a second point on a dose curve. The comparison between the two forms is covered on the sibling page on potassium nitrate mouthwash versus toothpaste.

Has anyone tested a different concentration?

Not in a toothpaste. This page ran the searches rather than assuming, and the terms are here so that anyone can repeat them.

Search, exactly as run against PubMed on 2026-09-10RecordsWhat came back
`("potassium nitrate"[tiab]) AND (dentifrice[tiab] OR toothpaste[tiab]) AND ("dose-response"[tiab] OR "dose response"[tiab] OR "concentration-dependent"[tiab] OR "dose-ranging"[tiab])`1an in situ erosion and remineralisation study of a test dentifrice
`"8% potassium nitrate"[tiab] OR "8 % potassium nitrate"[tiab]`0nothing at all
`"10% potassium nitrate"[tiab] OR "10 % potassium nitrate"[tiab]`6a laboratory study of a dental cement, three bleaching studies, a laser trial and a desensitising gel
`("3% potassium nitrate"[tiab] OR "3 % potassium nitrate"[tiab]) AND (dentifrice[tiab] OR toothpaste[tiab])`6five reports of the 3% mouthrinse and one enamel-softening study
`("potassium nitrate"[tiab]) AND (gel[tiab] OR varnish[tiab]) AND (concentration[tiab] OR concentrations[tiab])`17mostly bleaching studies; one of them is the trial below

The last of those five searches is the one that found something, and it is the closest anyone has come. A randomised trial published in 2003 gave 45 patients a bioadhesive gel containing either 5% or 10% potassium nitrate, or a placebo gel, and measured the response to a blast of air over fourteen days: at 48 hours the reduction was 35.8 per cent with the 10% gel against 11.8 per cent with the 5% gel and 13.4 per cent with placebo, and the gap between the concentrations reached significance at 96 hours11. On the tactile measure and on the patients' own ratings there was no significant difference between any of the three. The authors describe their own results as preliminary, the groups held fifteen patients each, and a gel left on the tooth is not a paste brushed on and spat out. It is a real dose comparison, and it is the only one; it cannot be carried across to a tube.

The design is not impossible, which is what makes its absence a finding rather than an oversight. A triple-blind split-mouth randomised trial in 31 patients compared potassium oxalate gels at 5% and 10% over twelve months and found the higher concentration held its effect longer, separating at nine and twelve months12. Somebody ran the dose comparison for a different potassium salt, followed the patients for a year and published it. For potassium nitrate in a toothpaste, the equivalent trial — three arms, the same base, three concentrations, one stimulus, eight weeks — has never been published. Until it is, "how much potassium nitrate is enough" has no evidence-based answer, and any pack that implies one is going beyond what has been measured.

Do two pastes with the same 5% deliver the same potassium?

There is good laboratory reason to think not, and no clinical evidence either way. This is a mechanism question, and everything in this section is laboratory work on extracted teeth or on dentine specimens: none of it says a person felt better.

The clearest sign comes from a manufacturer's own account of its development programme. A 2004 paper from a manufacturer's research centre describes building a 5% potassium nitrate dentifrice intended to improve on the market leader of the time, which also contained 5% potassium nitrate, and reports that the objective was met through what the authors call a new activated silica technology that raised potassium ion activity in laboratory testing13. The whole effort went into the base. The concentration was fixed, because the concentration was the one the trials had used.

Two further laboratory results sit behind that. In an in vitro model, potassium nitrate moved quickly through the dentine matrix out of a silica-based paste, and the deposit left on the dentine was a mixture of copolymer and silica rather than the potassium salt, in work by authors at the same manufacturer's research centre14. And when 50 extracted human molars were treated for thirty minutes with four different potassium nitrate materials and the pulp cavity was measured by spectrophotometry, the amount of nitrate that arrived differed significantly between the formulations, with the toothpaste giving the highest median reading and the most penetrating material the least viscous15. Extracted teeth have no pulpal pressure and no outward fluid flow, so this is a statement about formulations, not about mouths.

The trial literature has the same variety inside it. A scoping review of 138 randomised trials catalogued 368 toothpaste formulations and found potassium compounds in 68 of them, the largest single group of actives; across the whole set, silica-based and calcium-based abrasives and two fluoride salts, monofluorophosphate and sodium fluoride, account for most of the formulations16. The same active at the same level is not the same paste, and the reviews that pool those trials are pooling that variety.

One clinical trial comes as close to isolating it as anything published. In an eight-week randomised trial with 118 completers, funded by a manufacturer whose employees are among the authors, an experimental paste combining 3% copolymer with 5% potassium nitrate reduced cold-air and tactile scores more than a paste carrying the same 5% potassium nitrate alone, at every measured point from week two, while the patients' own pain ratings separated none of the four arms10. Held constant across those arms was the potassium; what changed was everything around it.

What did the 5% trials actually find?

A mixed record that improves on the examiner's measures more often than on the patient's, and syntheses that disagree with each other about what the pooled result is worth.

TrialDesign, size and funding, as recordedThe 5% paste was compared withLengthWhat it found
Nagata 1994double-blind randomised, 36 adults; funding not stated in the record1a matching placebo paste12 weekssignificant improvement on all three measures at weeks four, eight and twelve; complete relief of symptoms in 67% against 6%
Schiff 1994randomised, 67 adults; funding not stated in the record2a matching placebo without the potassium12 weekssignificant improvement on tactile, thermal and air-blast measures at six and twelve weeks
Schiff 1998randomised, 48 adults; funding not stated in the record3a placebo without the potassium8 weekssignificant improvement on tactile and thermal measures at four and eight weeks
Silverman 1996multicentre randomised, size not stated in the abstract; funding not stated in the record4placebo, and two marketed desensitising pastes4 weekssignificant reductions against placebo on all indexes
Wara-aswapati 2005randomised, 102 adults; funding not stated in the record7a fluoride-only paste12 weeksboth potassium arms beat the fluoride-only control on tactile and air measures
Salian 2010double-blind randomised, 30 adults, with a companion in vitro study; funding not stated in the record5a bioactive glass paste, and a non-desensitising paste4 weeksahead of the control paste on air and cold water at four weeks; the glass paste ahead of it at two and four weeks
Sharma 2010double-blind randomised, 120 adults; funding not stated in the record6a bioactive glass paste and a stannous fluoride gel, no placebo12 weeksair and water scores fell 35% and 34% by week two and 84% and 79% by week twelve; the glass paste ahead at two and four weeks
Elias-Boneta 2013double-blind randomised, 120 enrolled; manufacturer-sponsored, manufacturer authors8an arginine regimen, and a fluoride control regimen8 weeksair-blast scores improved significantly; the tactile measure did not improve significantly at any point
Biesbrock 2025double-blind randomised, 120 randomised; industry-funded, manufacturer employees9stannous fluoride, an oxalate paste, a fluoride control8 weeks, then 3 weeks offahead of the control on the cold-air score at every point, 44% better at week eight; tactile not significant at day three
Seong 2026randomised examiner-blind, 118 completers; industry-funded, manufacturer employees10a copolymer paste, a copolymer-plus-potassium paste, a fluoride control8 weeksbehind the copolymer-plus-potassium paste from week two on both examiner measures; no arm separated on self-reported pain

Read the findings column and the pattern is the one the syntheses argue about. Six randomised trials went into the 2006 Cochrane review and a split verdict came out: significant improvement on the air blast and on the tactile threshold at six to eight weeks, nothing on the patients' own assessments, and reviewers who would not say the pooled result settled the question20. A 2015 meta-analysis of 31 randomised trials put potassium toothpastes ahead of placebo with a standardised mean difference of −1.28, and reported heterogeneity between trials of 86 to 95%21. A 2020 network meta-analysis of 125 randomised trials in 12,541 patients found potassium ahead of fluoride paste on the tactile stimulus with moderate certainty22. A 2017 network meta-analysis of nine trials found only a tendency towards relief for potassium nitrate formulations, without reaching significance24. In a 2019 network meta-analysis, potassium and placebo did not separate25. And a 2026 systematic review and network meta-analysis of 93 randomised trials rated potassium's two-week effect small and low-confidence, while the only high-confidence node in its network was stannous fluoride, which S3 does not contain23.

Those six syntheses read the same underlying trials. Averaging them would be dishonest. The honest summary is that the examiner's measures improve in most of these randomised trials, the patients' own ratings often do not, and the reviewers who have pooled the same evidence disagree about whether what is left is worth calling an effect2023. Two of the randomised trials in the table had no placebo arm at all67, so part of what they record cannot be separated from the act of being treated. Whichever synthesis is right, none of them is about a concentration: they had only one to pool. The full reading of the Cochrane review is on the sibling page on what the Cochrane review found and what it did not, and how the actives rank against one another is on nerve-calming actives compared.

What does S3 declare, and why does declaring it matter more than the number?

S3 declares 5% potassium nitrate, and that is a decision to match the published evidence rather than a claim to beat the tube next to it. Five per cent is the concentration the trials happened to use; nobody has shown it to be better than three or eight or ten in a paste, because nobody has compared them. Anyone reading this page for permission to believe that a declared 5% is stronger than an undeclared one should not take it: the level is the label, not the formulation, and a manufacturer's own laboratory work, set out above, says the base can change how much potassium is actually available from an identical declared level1315. A paste that publishes nothing may hold the same amount, or more, or less. What can be said is narrower and duller: with a published level you can check the tube against the trials, and with a blank you cannot.

The same applies to the other percentages on this pack. Both of the hydroxyapatite figures, 10% and 5%, are inclusion levels of the ingredient as supplied rather than active content, which is lower, and S3 publishes the two numbers side by side. A brand publishing figures to look impressive would leave the second one out.

One more thing this page will not soften. In an eight-week randomised trial in 101 adults that held the 5% constant and changed only the fluoride salt beside it, the arm carrying stannous fluoride came out ahead of the arm carrying sodium monofluorophosphate on tactile and air-blast measures at four and eight weeks; the test product was the manufacturer's own, and the record does not state who funded the trial17. Two further eight-week randomised trials of that same test paste, published the same year, put it ahead of a paste combining the same 5% with sodium fluoride1819. Sodium monofluorophosphate is the fluoride salt S3 uses, chosen for a reason that has nothing to do with the nerve: it does not react with the calcium in hydroxyapatite inside the tube. That comparison is on the record and it is not softened here, because it illustrates this page's argument better than any level on any pack does: what the potassium travels with has moved outcomes, and the potassium itself has never been tested at another level.

Potassium nitrate is also not the whole of what a sensitive tooth needs. Hydroxyapatite occludes and potassium desensitises; neither does the other's job. What either of them does takes weeks, not days: relief from this class of active is judged at two to four weeks, which is set out on the sibling page on how long potassium nitrate takes to work, and the mechanism itself — still unconfirmed in an intact human tooth — on how potassium nitrate is thought to calm a tooth. The Journal keeps a ranked view of the category, which is a different exercise from this one, and how sensitive toothpastes work explains what happens once any of these actives reaches the tooth.

When is severe sensitivity not a toothpaste question at all?

When it fits a pattern that a toothpaste was never tested against. Four patterns on the Oral Health Foundation's list send a person to a dentist rather than to a shelf: pain that is severe, sensitivity that has lasted more than a few weeks, a single affected tooth, and pain that arrived suddenly. Any of them can signal decay, a cracked tooth, gum problems or infection26. A dentist has options a shelf does not: a desensitising treatment applied to the tooth, a high-fluoride toothpaste on prescription, a filling over a worn area at the gumline, or treatment of the gum disease underneath. The NHS puts a plainer limit on waiting: see a dentist for toothache lasting more than two days, or toothache that painkillers do not settle27.

That is worth holding beside the hunt for a bigger number. The randomised trials on this page recruited people with dentine hypersensitivity — the short, sharp response to cold air or a cold drink, usually across several teeth — and measured them with a calibrated air blast and a probe over eight to twelve weeks16. Pain that lingers, throbs, wakes you or sits in one tooth was not what was being treated in any of them. A reader who has arrived here because the pain is bad enough to go looking for the strongest thing on the shelf may be looking on the wrong shelf entirely, and the fastest route to relief in that case is an appointment.

Frequently asked questions

Why do most packs not state how much potassium nitrate they contain?

Because nothing requires them to. A cosmetic toothpaste must publish its ingredient list, and most packs add a fluoride figure, but the level of a desensitising active is left to the brand. Nine of the twelve rows carrying potassium nitrate in the September 2026 category review publish no level. That is a labelling choice and nothing more: an undeclared level is not evidence of a low one, and this page does not read it as one.

Would 10% potassium nitrate work better than 5% in a toothpaste?

Nobody knows, and anyone who tells you otherwise is extrapolating. The comparison has never been made in a paste. It has been made once, in a randomised trial of two bioadhesive gels, where the 10% gel reduced the response to an air blast more than the 5% gel in the first four days, with no difference on the tactile measure or on what the patients themselves reported, in 45 people over fourteen days11. A gel that sits on the tooth and a paste that is brushed on and spat out are different products, and one preliminary trial in fifteen patients per group is not a dose curve.

Is S3 stronger than a paste that does not state its potassium nitrate level?

No one can say, including us. The other paste's level is not published, so there is nothing to compare; what differs is that S3's is. A declared level does not make a formula work better — a manufacturer's own laboratory work, above, suggests the base can change how much potassium is available from an identical declared level13 — it only makes the claim checkable against the trials that used the same figure.

Can a dentist give you something stronger than a shelf paste?

A dentist can do things a paste cannot, which is not the same as a bigger dose in a tube. The Oral Health Foundation lists a desensitising treatment applied directly to the tooth, a high-fluoride toothpaste on prescription, a filling over a worn area near the gumline and treatment of gum disease among what a dentist may do26. The extra strength in a prescription paste is fluoride, aimed at decay risk, not a bigger dose of a desensitising active.

Where S3 sits

S3 is formulated at inclusion levels that match the published studies: 5% potassium nitrate, and a 10% nano-hydroxyapatite solution. Those percentages are inclusion levels of the ingredient as supplied rather than active content, and S3 publishes both figures. The number worth looking for on any pack is not a bigger one, since nobody has ever published the comparison that would make a bigger one mean anything; it is a stated one, which is the only kind a reader can check.

S3 Sensitivity Science™ pairs potassium nitrate with two hydroxyapatites and adult-strength fluoride in one daily paste.

See the toothpaste

S3 Sensitivity Science™ carries three actives in one tube — potassium nitrate for the nerve, nano-hydroxyapatite inside the tubule and biomimetic hydroxyapatite on the surface, at 10% and 5% as supplied — and keeps 1450 ppm fluoride with them. One tube doing three jobs: calming the nerve, strengthening the enamel surface, and protecting against further wear. The formulation is patent-pending as S3 Repair Technology™, UK application GB2604755.5. More than 20 practising UK dentists own a stake in S3, and nine founding dentists advise on the formulation. Read more about S3.

References 27 sources

1
Nagata T, Ishida H, Shinohara H, Nishikawa S, Kasahara S, Wakano Y, Daigen S, Troullos ES. Clinical evaluation of a potassium nitrate dentifrice for the treatment of dentinal hypersensitivity. Journal of Clinical Periodontology. 1994;21(3):217-221. doi:10.1111/j.1600-051x.1994.tb00307.x Double-blind randomised trial, 36 adults.
2
Schiff T, Dotson M, Cohen S, De Vizio W, McCool J, Volpe A. Efficacy of a dentifrice containing potassium nitrate, soluble pyrophosphate, PVM/MA copolymer, and sodium fluoride on dentinal hypersensitivity: a twelve-week clinical study. The Journal of Clinical Dentistry. 1994;5 Spec No:87-92. PMID 8534380. Randomised trial, 67 adults.
3
Schiff T, Dos Santos M, Laffi S, Yoshioka M, Baines E, Brasil KD, McCool JJ, De Vizio W. Efficacy of a dentifrice containing 5% potassium nitrate and 1500 ppm sodium monofluorophosphate in a precipitated calcium carbonate base on dentinal hypersensitivity. The Journal of Clinical Dentistry. 1998;9(1):22-25. PMID 9835829. Randomised trial, 48 adults.
4
Silverman G, Berman E, Hanna CB, Salvato A, Fratarcangelo P, Bartizek RD, Bollmer BW, Campbell SL, Lanzalaco AC, Mackay BJ, McClanahan SF, Perlich MA, Shaffer JB. Assessing the efficacy of three dentifrices in the treatment of dentinal hypersensitivity. Journal of the American Dental Association. 1996;127(2):191-201. doi:10.14219/jada.archive.1996.0169 Multicentre randomised trial, size not stated in the abstract.
5
Salian S, Thakur S, Kulkarni S, LaTorre G. A randomized controlled clinical study evaluating the efficacy of two desensitizing dentifrices. The Journal of Clinical Dentistry. 2010;21(3):82-87. PMID 21207919. Double-blind randomised trial with companion in vitro electron microscopy, 30 adults.
6
Sharma N, Roy S, Kakar A, Greenspan DC, Scott R. A clinical study comparing oral formulations containing 7.5% calcium sodium phosphosilicate (NovaMin), 5% potassium nitrate, and 0.4% stannous fluoride for the management of dentin hypersensitivity. The Journal of Clinical Dentistry. 2010;21(3):88-92. PMID 21207920. Double-blind randomised trial, 120 adults.
7
Wara-aswapati N, Krongnawakul D, Jiraviboon D, Adulyanon S, Karimbux N, Pitiphat W. The effect of a new toothpaste containing potassium nitrate and triclosan on gingival health, plaque formation and dentine hypersensitivity. Journal of Clinical Periodontology. 2005;32(1):53-58. doi:10.1111/j.1600-051X.2004.00631.x Randomised trial, 102 adults.
8
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9
Biesbrock AR, He T, Zou Y, Grender JM, Amini P, Sagel PA, Groth A, Klukowska M. Randomized clinical trial evaluating kinetic benefits of desensitizing agents: magnitude, onset, and stability of relief. Journal of Periodontology. 2025;96(12):1339-1351. doi:10.1002/JPER.24-0688 Double-blind randomised trial, 120 randomised.
10
Seong J, Parkinson C, Mangal M, Grimaldi R, Serra G, Smith G, Karandikar Y, West N. An exploratory randomised controlled clinical trial to evaluate the efficacy of an experimental toothpaste in the relief of dentine hypersensitivity. Journal of Dentistry. 2026;164:106226. doi:10.1016/j.jdent.2025.106226 Randomised examiner-blind trial, 118 completers.
11
Frechoso SC, Menéndez M, Guisasola C, Arregui I, Tejerina JM, Sicilia A. Evaluation of the efficacy of two potassium nitrate bioadhesive gels (5% and 10%) in the treatment of dentine hypersensitivity. A randomised clinical trial. Journal of Clinical Periodontology. 2003;30(4):315-320. doi:10.1034/j.1600-051x.2003.20077.x Randomised trial, 45 patients.
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Galvão ADM, Zeola LF, Moura GF, Teixeira DNR, Gonzaga RCQ, da Silva GR, Soares PV. A long-term evaluation of experimental potassium oxalate concentrations on dentin hypersensitivity reduction: a triple-blind randomized clinical trial. Journal of Dentistry. 2019;89:103180. doi:10.1016/j.jdent.2019.103180 Split-mouth randomised trial, 31 patients, twelve months.
13
Tavss EA, Fisher SW, Campbell S, Bonta Y, Darcy-Siegel J, Blackwell BL, Volpe AR, Miller SE. The scientific rationale and development of an optimized dentifrice for the treatment of dentin hypersensitivity. American Journal of Dentistry. 2004;17(1):61-70. PMID 15241912. Laboratory and analytical development report.
14
Miller S, Gaffar A, Sullivan R, Heu R, Truong T, Stranick M. Evaluation of a new dentifrice for the treatment of sensitive teeth. The Journal of Clinical Dentistry. 1994;5 Spec No:71-79. PMID 8534377. In vitro study on dentine specimens.
15
Kwon SR, Dawson DV, Schenck DM, Fiegel J, Wertz PW. Spectrophotometric evaluation of potassium nitrate penetration into the pulp cavity. Operative Dentistry. 2015;40(6):614-621. doi:10.2341/14-214-L In vitro study, 50 extracted human molars.
16
Martins CC, Riva JJ, Firmino RT, Schünemann HJ. Formulations of desensitizing toothpastes for dentin hypersensitivity: a scoping review. Journal of Applied Oral Science. 2022;30:e20210410. doi:10.1590/1678-7757-2021-0410 Systematic scoping review, 138 randomised trials and 368 formulations.
17
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18
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19
Sowinski JA, Battista GW, Petrone ME, Chaknis P, Zhang YP, DeVizio W, Volpe AR, Proskin HM. A new desensitizing dentifrice: an eight-week clinical investigation. Compendium of Continuing Education in Dentistry Supplement. 2000;(27):11-16. PMID 11908355. Double-blind randomised trial, 109 adults.
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21
Bae JH, Kim YK, Myung SK. Desensitizing toothpaste versus placebo for dentin hypersensitivity: a systematic review and meta-analysis. Journal of Clinical Periodontology. 2015;42(2):131-141. doi:10.1111/jcpe.12347 Systematic review and meta-analysis, 31 randomised trials.
22
Martins CC, Firmino RT, Riva JJ, Ge L, Carrasco-Labra A, Brignardello-Petersen R, Colunga-Lozano LE, Granville-Garcia AF, Costa FO, Yepes-Nuñez JJ, Zhang Y, Schünemann HJ. Desensitizing toothpastes for dentin hypersensitivity: a network meta-analysis. Journal of Dental Research. 2020;99(5):514-522. doi:10.1177/0022034520903036 Systematic review and network meta-analysis, 125 randomised trials, 12,541 patients.
23
Gormley AJ, Walsh T, Twigg J, Farrugia C, Pollard A, Bullock B, West NX. Dentifrice formulations for the treatment of dentin hypersensitivity: a systematic review and network meta-analysis. Periodontology 2000. 2026. doi:10.1111/prd.70088 Systematic review and network meta-analysis, 93 randomised trials, 9,548 participants.
24
Grünberg C, Bauer F, Crispin A, Jakob M, Hickel R, Draenert ME. Effectiveness of dentifrices with new formulations for the treatment of dentin hypersensitivity: a meta-analysis. American Journal of Dentistry. 2017;30(4):221-226. PMID 29178705. Systematic review and network meta-analysis, nine randomised trials.
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Hu ML, Zheng G, Lin H, Yang M, Zhang YD, Han JM. Network meta-analysis on the effect of desensitizing toothpastes on dentine hypersensitivity. Journal of Dentistry. 2019;88:103170. doi:10.1016/j.jdent.2019.07.008 Systematic review and network meta-analysis, 30 randomised trials.
26
Oral Health Foundation. Sensitive teeth. https://www.dentalhealth.org/sensitive-teeth Accessed 2026-09-10.
27
NHS. Toothache. https://www.nhs.uk/symptoms/toothache/ Accessed 2026-09-10.