Study Evaluating DVS-233 SR for Treatment of Vasomotor Symptoms Associated With Menopause

Mise à jour : Il y a 4 ans
Référence : NCT00195546

Femme Homme

Extrait

Primary: To assess the efficacy and safety of DVS-233 SR compared with placebo for treatment of vasomotor symptoms (VMS) associated with menopause and to compare the bleeding incidence of DVS-233 SR and tibolone. Secondary: To assess the effects of DVS-233 SR and tibolone on changes from baseline in weight, breast pain, and health outcomes indicators.


Critère d'inclusion

  • Menopause


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