Clinical trial
Study on Safety and Efficacy of an Oral Contraceptive in Treating Acne…
NCT00280657 · Bayer, Industry · Completed
Key facts
| NCT number | NCT00280657 |
|---|---|
| Title | Study on Safety and Efficacy of an Oral Contraceptive in Treating Acne Papulopustulosa |
| Official title | Multicenter, Double-blind, Double-dummy, Randomized Parallel Group Study to Evaluate the Safety and Efficacy of SH D 00659 E for 6 Treatment Cycles in Female Patients With Acne Papulopustulosa in Comparison to SH D 00659 G and Placebo. |
| Lead sponsor | Bayer, Industry |
| Status | Completed |
| Phase | Phase 3 |
| Study type | Interventional |
| Conditions | Acne Vulgaris |
| Intervention type | Drug |
| Interventions | Valette, Diane, Placebo |
| Enrollment | 1,326 |
| Start date | Mar 10, 2004 |
| Primary completion | May 21, 2005 |
| Completion | May 21, 2005 |
| First posted | Jan 23, 2006 |
| Last update posted | Jun 6, 2023 |
| Countries | Czechia, Poland, Russia, Slovakia, Ukraine |
At a glance
- No Results posted
- None Linked FDA submissions
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date: