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Completed Phase 4 Interventional

Sexual Functioning Study With Antidepressants

ClinicalTrials.gov ID: NCT00316160

Public ClinicalTrials.gov record NCT00316160. 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 13, 2026, 3:52 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 Twelve-week, Multi-center, Randomized, Double-blind, Double-dummy, Parallel-group, Active Controlled, Escalating Dose Study to Compare the Effects on Sexual Functioning of Bupropion Hydrochloride Extended-release (WELLBUTRIN XL, 150-450 mg/Day) and Extended-release Venlafaxine (EFFEXOR XR, 75-225 mg/Day) in Subjects With Major Depressive Disorder

Study identification

NCT ID
NCT00316160
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
347 participants

Conditions and interventions

Interventions

  • Bupropion Hydrochloride Extended-release Drug
  • Extended-release Venlafaxine Drug

Drug

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
Aug 31, 2004
Primary completion
Apr 30, 2005
Completion
Apr 30, 2005
Last update posted
May 29, 2017

2004 – 2005

United States locations

U.S. sites
45
U.S. states
24
U.S. cities
43
Facility City State ZIP Site status
GSK Investigational Site Mesa Arizona 85210
GSK Investigational Site Phoenix Arizona 85023
GSK Investigational Site Scottsdale Arizona 85251
GSK Investigational Site Little Rock Arkansas 72223
GSK Investigational Site Beverly Hills California 90210
GSK Investigational Site Burbank California 91506
GSK Investigational Site La Mesa California 91942
GSK Investigational Site San Francisco California 94109
GSK Investigational Site Temecula California 92591
GSK Investigational Site Upland California 91786
GSK Investigational Site Walnut Creek California 94598
GSK Investigational Site Denver Colorado 80212
GSK Investigational Site Coral Springs Florida 33065
GSK Investigational Site Jacksonville Florida 32216
GSK Investigational Site Orlando Florida 32806
GSK Investigational Site Marietta Georgia 30060
GSK Investigational Site Smyrna Georgia 30080
GSK Investigational Site Oak Brook Illinois 60523
GSK Investigational Site Indianapolis Indiana 46202
GSK Investigational Site New Orleans Louisiana 70112
GSK Investigational Site Rockville Maryland 20852
GSK Investigational Site Braintree Massachusetts 02184
GSK Investigational Site Greenfield Massachusetts 01301
GSK Investigational Site Minneapolis Minnesota 55454
GSK Investigational Site Las Vegas Nevada 89146
GSK Investigational Site Brooklyn New York 11235
GSK Investigational Site New York New York 10128
GSK Investigational Site Charlotte North Carolina 28209
GSK Investigational Site Cleveland Ohio 44109
GSK Investigational Site Toledo Ohio 43623
GSK Investigational Site Oklahoma City Oklahoma 73112
GSK Investigational Site Oklahoma City Oklahoma 73117
GSK Investigational Site Eugene Oregon 97401
GSK Investigational Site Portland Oregon 97209
GSK Investigational Site Portland Oregon 97210
GSK Investigational Site Lincoln Rhode Island 02865-4208
GSK Investigational Site Charleston South Carolina 29407
GSK Investigational Site Columbia South Carolina 29201
GSK Investigational Site Austin Texas 78756
GSK Investigational Site Bellaire Texas 77401
GSK Investigational Site Fort Worth Texas 76107
GSK Investigational Site San Antonio Texas 78229
GSK Investigational Site Charlottesville Virginia 22908
GSK Investigational Site Yakima Washington 98902
GSK Investigational Site Middleton Wisconsin 53562-2215

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 NCT00316160, 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 29, 2017 · Synced May 13, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00316160 live on ClinicalTrials.gov.

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