Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT00161681Phase 3Completed
Phase 3, randomised, double-blind trial in premenstrual syndrome (PMS) comparing Levonorgestrel/Ethinyl Estradiol with Placebo (2 arms). Primary endpoint: Efficacy in preventing moderate to severe cycle-related symptoms. Started Jul 2005; status: completed.
Beyond the preview
Study design, results and competitive context are available in the Gosset platform where reported.
Available in the Gosset platform where reported.
Available in the Gosset platform where reported.
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