Trials / Completed
CompletedNCT02613117
Research on Oral Tolerability and Product Application/Response of Two Oxalate Products for Dental Patients With Risk of Dentinal Hypersensitivity
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 104 (actual)
- Sponsor
- Procter and Gamble · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Accepted
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.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Potassium Oxalate Gel | Self applied |
| DEVICE | Potassium Oxalate Liquid | Professionally Applied |
| DRUG | Stannous fluoride paste | SnF2 Paste |
Timeline
- Start date
- 2015-11-01
- Primary completion
- 2016-06-01
- Completion
- 2016-06-01
- First posted
- 2015-11-24
- Last updated
- 2020-09-22
- Results posted
- 2020-09-22
Locations
1 site across 1 country: United States
Source: ClinicalTrials.gov record NCT02613117. Inclusion in this directory is not an endorsement.