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NCT01592864 · ClinicalTrials.gov registry record · Phase 3
The Efficacy of a Dentifrice in Providing Relief From the Pain of Dentinal Hypersensitivity
A Phase 3 study, sponsored by GlaxoSmithKline.
- Completed
- Registry status
- Phase 3
- Development phase
- 120
- Enrollment target
NCT01592864: Completed Phase 3 study, sponsored by GlaxoSmithKline.
NCT01592864 is a Phase 3 study that has completed, run by GlaxoSmithKline. The registered enrollment target is 120 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (84% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01592864, a Phase 3 study, has completed, sponsored by GlaxoSmithKline.
- COMPLETED
- Registry status
- Phase 3
- Development phase
- 120 participants
- Enrollment target
Study Summary
A study to compare the efficacy of a test dentifrice against a control dentifrice in reducing dentinal hypersensitivity over an eight week treatment period.
Primary Outcome
Response to a constant jet of air applied to hypersensitive teeth is evaluated using a Schiff Sensitivity pain response scale. According to this analog scale, pain response for each individual stimulated tooth ranged from 0 to 3; 0 - participant does not respond to air stimulation, 1 - participant responds to air stimulus but does not request discontinuation of stimulus, 2 - participant responds to air stimulus and request discontinuation of stimulus, 3 - participant responds to air stimulus, co
Interventions
- DRUG Stannous Fluoride
- DRUG Sodium Monofluorophosphate
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 120 participants |
| Start Date | 2012-03 |
| Est. Completion | 2012-05 |
| Phase | Phase 3 |
What the finished NCT01592864 record still lists
NCT01592864 is an interventional study that assigns participants to a tested intervention. The registered 120 participants enrollment target is mid-sized for trials with a published cap, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (84% lower).
The record links to 0 conditions, and to 2 interventions - of which Stannous Fluoride is the first listed.
NCT01592864 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01592864 about?
NCT01592864 is a clinical study titled "The Efficacy of a Dentifrice in Providing Relief From the Pain of Dentinal Hypersensitivity". A study to compare the efficacy of a test dentifrice against a control dentifrice in reducing dentinal hypersensitivity over an eight week treatment period.
What is the current status of trial NCT01592864?
This trial is currently completed. It is a Phase 3 study. The enrollment target is 120 participants. The study started on 2012-03. Estimated completion is 2012-05.
What interventions are being tested in trial NCT01592864?
The interventions under investigation include: Stannous Fluoride (DRUG), Sodium Monofluorophosphate (DRUG).
Who is sponsoring clinical trial NCT01592864?
This trial is sponsored by GlaxoSmithKline, which has 1,345 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01592864's enrollment target sits among peer trials
120 1619th of 2000 higher than 361 of 2,000 other Phase 3 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 3 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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