Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT00256685Phase 3Completed
Phase 3, randomised, double-blind trial in vasomotor symptoms comparing Desvenlafaxine Succinate with Placebo (2 arms). Primary endpoints: Reduction in average daily number of moderate & severe hot flushes at 12 weeks and Reduction in average daily severity score at 12 weeks. Started Sep 2004; 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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