At a glance
ClinicalIndex Comparison RecordN/ACompleted· 100 enrolled
Drug / intervention
ClōSYS® Unflavored Rinse +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.
Efficacy of ClōSYS® Oral Rinse Products in Human Subjects in Controlling Oral Malodor
In Brief
A clinical study evaluating ClōSYS® Unflavored Rinse, ClōSYS® Flavored Rinse, and 1 other intervention for Oral Malodor. Completed, enrolled 100 participants.
Detailed Summary
The purpose of this Study is to assess the efficacy of two ClōSYS Oral Rinse products in human subjects in controlling oral malodor in partial fulfillment of the requirements for American Dental Association's (ADA) requirement for obtaining ADA Seal for malodor.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsOral Malodor
Countries--
CollaboratorsLoma Linda University
Timeline
N/ACompletedFinished
2017201820192020202120222023202420252026
Enrollment StartAug 2016
Primary CompletionNov 2016
First PostedMay 2017
TodayJul 2026
First PostedMay 19, 2017
Enrollment StartAug 1, 2016
Primary CompletionNov 1, 2016
TodayJul 2, 2026
Enrollment to primary: 3 monthsPosted 9.1 years ago
Interventions
ClōSYS® Unflavored Rinsedrug
Subjects in Test group will receive ClōSYS® Unflavored Rinse.
ClōSYS® Flavored Rinsedrug
Subjects in Test group will receive ClōSYS® Flavored Rinse.
Placeboother
Subjects in Placebo group will receive Placebo Rinse.