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Completed Phase 3 Interventional

Effects Of Antidepressants On Sexual Functioning In Adults

ClinicalTrials.gov ID: NCT00051272

Public ClinicalTrials.gov record NCT00051272. 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 26, 2026, 1:47 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, Double-blind Randomized Placebo-controlled Comparison of the Effects on Sexual Functioning of Extended-release Bupropion Hydrochloride (300-450mg) and Escitalopram (10-20mg) in Outpatients With Moderate to Severe Major Depression Over an Eight-Week Treatment Period

Brief summary

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

This study will evaluate the effects of two antidepression medications on sexual functioning.

Study identification

NCT ID
NCT00051272
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
425 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
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
Jan 2003 (Type not available)
Primary completion
Jun 2004 (Actual)
Completion
Jun 2004 (Actual)
Last update posted
Mar 29, 2011

2003 – 2004

United States locations

U.S. sites
24
U.S. states
19
U.S. cities
22
Facility City State ZIP Site status
GSK Investigational Site Phoenix Arizona 85015 —
GSK Investigational Site Scottsdale Arizona 85251 —
GSK Investigational Site Berkeley California 94709 —
GSK Investigational Site Middletown Connecticut 06457 —
GSK Investigational Site Wilmington Delaware 19808 —
GSK Investigational Site Washington D.C. District of Columbia 20037 —
GSK Investigational Site Orlando Florida 32806 —
GSK Investigational Site Marietta Georgia 30060 —
GSK Investigational Site Smyrna Georgia 30080 —
GSK Investigational Site Boise Idaho 83702 —
GSK Investigational Site Baton Rouge Louisiana 70808 —
GSK Investigational Site Braintree Massachusetts 02184 —
GSK Investigational Site Piscataway New Jersey 08854 —
GSK Investigational Site New York New York 10128 —
GSK Investigational Site Raleigh North Carolina 27609 —
GSK Investigational Site Cleveland Ohio 44106 —
GSK Investigational Site Oklahoma City Oklahoma 73118 —
GSK Investigational Site Nashville Tennessee 37203 —
GSK Investigational Site Bellaire Texas 77401 —
GSK Investigational Site San Antonio Texas 78229-3815 —
GSK Investigational Site San Antonio Texas 78229 —
GSK Investigational Site San Antonio Texas — —
GSK Investigational Site Salt Lake City Utah 84107 —
GSK Investigational Site Yakima Washington 98902 —

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 NCT00051272, 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 Mar 29, 2011 · Synced Oct 26, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00051272 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →