Trials / Completed
CompletedNCT00793026
Dermacyd Breeze Pocket BR (Lactic Acid) - Acceptability
Safety Dermatological Evaluation: Genital Mucous Irritation - Test in Use - Dermacyd Breeze Pocket BR (Lactic Acid).
- Status
- Completed
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 30 (actual)
- Sponsor
- Sanofi · Industry
- Sex
- Female
- Age
- 18 Years – 60 Years
- Healthy volunteers
- Accepted
Summary
The purpose of this study is to prove the safety of the gynaecological formulation in normal conditions of use.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Dermacyd Breeze Pocket BR (Lactic Acid) | Dermacyd Breeze Pocket BR (Lactic Acid) during 21 consecutive days |
Timeline
- Start date
- 2008-11-01
- Primary completion
- 2008-11-01
- First posted
- 2008-11-18
- Last updated
- 2008-12-19
Locations
1 site across 1 country: Brazil
Source: ClinicalTrials.gov record NCT00793026. Inclusion in this directory is not an endorsement.