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Completed Phase 3 Interventional Results available

Study Evaluating Desvenlafaxine Succinate Sustained Release (DVS SR) vs. Escitalopram in Postmenopausal Women

ClinicalTrials.gov ID: NCT00406640

Public ClinicalTrials.gov record NCT00406640. 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 Oct 27, 2026, 12:55 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 Acute Phase Followed By a 6-Month Continuation Phase (Open-Label Or Double-Blind) Study to Evaluate the Efficacy, Safety, and Tolerability of DVS SR Versus Escitalopram in Postmenopausal Women With Major Depressive Disorder

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

Desvenlafaxine succinate (DVS) is a potent and selective serotonin and norepinephrine reuptake inhibitor (SNRI). This study will investigate the safety, efficacy, and tolerability of DVS SR versus escitalopram in women with major depressive disorder (MDD) who are postmenopausal.

Study identification

NCT ID
NCT00406640
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Enrollment
595 participants

Conditions and interventions

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
Dec 2006 (Type not available)
Primary completion
Feb 2008 (Actual)
Completion
Oct 2008 (Actual)
Last update posted
Dec 28, 2023

2006 – 2008

United States locations

U.S. sites
52
U.S. states
26
U.S. cities
49
Facility City State ZIP Site status
Not listed Peoria Arizona 85381 —
Not listed Pasadena California 91107 —
Not listed San Diego California 92103 —
Not listed San Diego California 92108 —
Not listed Denver Colorado 80212 —
Not listed Cromwell Connecticut 06416 —
Not listed Farmington Connecticut 06030 —
Not listed Waterbury Connecticut 06708 —
Not listed Brooksville Florida 34613 —
Not listed Coral Springs Florida 33065 —
Not listed Fort Myers Florida 33912 —
Not listed Gainesville Florida 32607 —
Not listed Maitland Florida 32751 —
Not listed Atlanta Georgia 30328 —
Not listed Roswell Georgia 30076 —
Not listed Northfield Illinois 60093 —
Not listed Oak Brook Illinois 60523 —
Not listed Overland Park Kansas 66211 —
Not listed Wichita Kansas 67214 —
Not listed New Orleans Louisiana 70115 —
Not listed Shreveport Louisiana 71130 —
Not listed Baltimore Maryland 21208 —
Not listed Boston Massachusetts 02114 —
Not listed Fall River Massachusetts 02721 —
Not listed Saint Paul Minnesota 55101 —
Not listed Las Vegas Nevada 89106 —
Not listed Piscataway New Jersey 08854 —
Not listed Elmsford New York 10523 —
Not listed Hollis New York 11423 —
Not listed New York New York 10032 —
Not listed New York New York 10128 —
Not listed Syracuse New York 13210 —
Not listed Raleigh North Carolina 27612 —
Not listed Oklahoma City Oklahoma 73103 —
Not listed Philadelphia Pennsylvania 19104 —
Not listed Pittsburgh Pennsylvania 15206 —
Not listed Pittsburgh Pennsylvania 15213 —
Not listed East Providence Rhode Island 02914 —
Not listed Lincoln Rhode Island 02865 —
Not listed Charleston South Carolina 29407 —
Not listed Columbia South Carolina 29201 —
Not listed Mt. Pleasant South Carolina 29464 —
Not listed Memphis Tennessee 38117 —
Not listed Bellaire Texas 77401 —
Not listed Dallas Texas 75235 —
Not listed Denton Texas 76201 —
Not listed Houston Texas 77090 —
Not listed Burlington Vermont 05401 —
Not listed Charlottesville Virginia 22903 —
Not listed Richmond Virginia 23230 —
Not listed Morgantown West Virginia 26506 —
Not listed Middleton Wisconsin 53562 —

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 18 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00406640, 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 Dec 28, 2023 · Synced Oct 27, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00406640 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →