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Completed Phase 3 Interventional Results available

Study Evaluating Desvenlafaxine Succinate Sustained Release (DVS SR) Versus Placebo in Peri- and Postmenopausal Women

ClinicalTrials.gov ID: NCT00369343

Public ClinicalTrials.gov record NCT00369343. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced May 19, 2026, 8:31 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Multicenter, Randomized, 8-week, Double-blind, Placebo-controlled Study Followed by a 6-month Open-label Extension to Evaluate the Efficacy and Safety of DVS SR in Peri- and Postmenopausal Women With Major Depressive Disorder

Study identification

NCT ID
NCT00369343
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Wyeth is now a wholly owned subsidiary of Pfizer
Industry
Enrollment
381 participants

Conditions and interventions

Interventions

  • Desvenlafaxine administered as a succinate salt in a sustained-release form (DVS SR) Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
40 Years to 70 Years
Sex
Female
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Aug 31, 2006
Primary completion
Oct 31, 2007
Completion
Jun 30, 2008
Last update posted
May 6, 2012

2006 – 2008

United States locations

U.S. sites
37
U.S. states
23
U.S. cities
36
Facility City State ZIP Site status
Not listed Birmingham Alabama 35226
Not listed Little Rock Arkansas 72223
Not listed Springdale Arkansas 72762
Not listed Palo Alto California 94305
Not listed San Diego California 92103
Not listed New London Connecticut 06320
Not listed Bradenton Florida 34208
Not listed Miami Florida 33133
Not listed Tampa Florida 33613
Not listed Winter Park Florida 32789
Not listed Atlanta Georgia 30308
Not listed Sandy Springs Georgia 30328
Not listed Savannah Georgia 31406
Not listed Smyrna Georgia 30080
Not listed Idaho Falls Idaho 83404
Not listed Chicago Illinois 60634
Not listed Indianapolis Indiana 46202
Not listed Terre Haute Indiana 47802
Not listed Shreveport Louisiana 71101
Not listed Rockville Maryland 20852
Not listed Omaha Nebraska 68131
Not listed Cherry Hill New Jersey 08002
Not listed Brooklyn New York 11235
Not listed Minot North Dakota 58701
Not listed Beachwood Ohio 44122
Not listed Dayton Ohio 45408
Not listed Toledo Ohio 43623
Not listed Oklahoma City Oklahoma 73118
Not listed Tulsa Oklahoma 74135
Not listed Philadelphia Pennsylvania 19131
Not listed Hilton Head Island South Carolina 29926
Not listed Austin Texas 78756
Not listed Houston Texas 77007
Not listed Richmond Virginia 23229
Not listed Richmond Virginia 23230
Not listed Seattle Washington 98105
Not listed Brown Deer Wisconsin 53223

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00369343, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted May 6, 2012 · Synced May 19, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00369343 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →