Study Evaluating The Safety And Efficacy Of Desvenlafaxine Succinate For Vasomotor Symptoms In Menopausal Women

Completed · Phase 3 · Has a placebo group

Conditions studied: Vasomotor Symptoms

In brief

The purpose of the study is to evaluate the efficacy and safety of Desvenlafaxine Succinate (DVS) Sustained Release (SR), in comparison to placebo for the treatment of Vasomotor Symptoms (VMS) in menopausal women.

Key facts

Study ID
NCT00683800
Run by
Pfizer
People needed
2186
Starts
2008-06-01
Expected to finish
2010-05-01
Last updated by the study team
2011-08-17

Who can join

Age: 45 and older. Sex: female. Healthy volunteers: accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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