Trials / Completed
CompletedNCT00590590
Safety and Efficacy of Two Vaginal Products Versus Placebo in Patients With Vaginal Discomfort
- Status
- Completed
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 105 (actual)
- Sponsor
- Lumara Health, Inc. · Industry
- Sex
- Female
- Age
- 18 Years – 50 Years
- Healthy volunteers
- Not accepted
Summary
This study will evaluate the efficacy and safety of two vaginal products compared with that of placebo to determine if the two products are better than placebo in the relief of vaginal discomfort.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Lidocaine/Diphenhydramine | semi solid, twice weekly, 4 months |
| DRUG | lidocaine | semi solid, twice weekly for 4 months |
| DRUG | placebo | semi solid, twice weekly for 4 months |
Timeline
- Start date
- 2007-10-01
- Primary completion
- 2009-06-01
- Completion
- 2009-07-01
- First posted
- 2008-01-10
- Last updated
- 2012-03-02
- Results posted
- 2011-02-09
Locations
48 sites across 2 countries: United States, Canada
Source: ClinicalTrials.gov record NCT00590590. Inclusion in this directory is not an endorsement.