At a glance
ClinicalIndex Comparison RecordN/ACompleted· 104 enrolled
Drug / intervention
Stannous fluoride paste +2 moredrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Research on Oral Tolerability and Product Application/Response of Two Oxalate Products for Dental Patients With Risk of Dentinal Hypersensitivity
In Brief
A clinical study evaluating Potassium Oxalate Gel, Potassium Oxalate Liquid, and 1 other intervention for Dentinal Hypersensitivity. Completed, enrolled 104 participants across 1 site.
Detailed Summary
This study will assess the oral tolerability and immediate post-treatment safety of topical application for two marketed oxalate products as initial care in dental patients to treat or prevent tooth sensitivity pain that may be attributed to dentinal hypersensitivity.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsDentinal Hypersensitivity
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
20162017201820192020202120222023202420252026
Enrollment StartNov 2015
First PostedNov 2015
Primary CompletionJun 2016
TodayJul 2026
First PostedNov 24, 2015
Enrollment StartNov 1, 2015
Primary CompletionJun 1, 2016
TodayJul 2, 2026
Enrollment to primary: 7 monthsPosted 10.6 years ago
Interventions
Potassium Oxalate Geldevice
Self applied
Potassium Oxalate Liquiddevice
Professionally Applied
Stannous fluoride pastedrug
SnF2 Paste