Trials / Completed
CompletedNCT00800293
Randomized Study to Compare the Bioavailability of Two Augmented Betamethasone Dipropionate 0.05% Topical Creams
Bioequivalence of Two Augmented Betamethasone Dipropionate 0.05% Topical Creams
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 116 (actual)
- Sponsor
- Padagis LLC · Industry
- Sex
- Female
- Age
- 18 Years – 50 Years
- Healthy volunteers
- Accepted
Summary
The purpose of this study was to compare the relative vasoconstrictive effects of test and reference topical augmented betamethasone dipropionate augmented 0.05% cream in healthy, female subjects.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Betamethasone Dipropionate 0.05% Cream | Small amount applied and evaluated over the course of several hours |
Timeline
- Start date
- 2002-12-01
- Primary completion
- 2003-01-01
- Completion
- 2003-01-01
- First posted
- 2008-12-02
- Last updated
- 2021-10-18
Source: ClinicalTrials.gov record NCT00800293. Inclusion in this directory is not an endorsement.