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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 Oct 27, 2026, 4:13 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

Brief summary

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

Effects of two depression medication on sexual functioning

Study identification

NCT ID
NCT00316160
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
347 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
Sep 2004 (Type not available)
Primary completion
May 2005 (Actual)
Completion
May 2005 (Actual)
Last update posted
May 30, 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 30, 2017 · Synced Oct 27, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00316160 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →