Study design & results
Available in the Gosset platform where reported.
Trial intelligence / Profile preview
NCT04081805Active, not recruiting
Randomised, open-label trial (3 arms), sponsored by Federal University of São Paulo. Primary endpoints: Clinical Improvement of signs and symptoms of vulvovaginal atrophy at 90 days and Satisfaction with treatment at 90 days. Started Sep 2019; status: active, not recruiting.
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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