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Completed Phase 3 Interventional

Prevention of Seasonal Affective Disorder

ClinicalTrials.gov ID: NCT00046241

Public ClinicalTrials.gov record NCT00046241. 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 Jul 23, 2026, 6:57 AM 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 7 Month, Multicenter, Randomized, Double-blind, Placebo-controlled Comparison of 150-300mg/Day of Extended-release Bupropion Hydrochloride and Placebo for the Prevention of Seasonal Affective Disorder in Subjects With a History of Seasonal Affective Disorder Followed by an 8-week Observational Follow-up Phase

Study identification

NCT ID
NCT00046241
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
300 participants

Conditions and interventions

Interventions

  • Extended-release bupropion hydrochloride 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, 2002
Primary completion
May 31, 2003
Completion
May 31, 2003
Last update posted
Jan 22, 2017

2002 – 2003

United States locations

U.S. sites
43
U.S. states
23
U.S. cities
40
Facility City State ZIP Site status
GSK Clinical Trials Call Center Anchorage Alaska 99508
GSK Clinical Trials Call Center Hamden Connecticut 06518
GSK Clinical Trials Call Center Boise Idaho 83702
GSK Clinical Trials Call Center Chicago Illinois 60637
GSK Clinical Trials Call Center Edwardsville Illinois 62025
GSK Clinical Trials Call Center Oak Brook Illinois 60523
GSK Clinical Trials Call Center Oakbrook Terrace Illinois 60181
GSK Clinical Trials Call Center Lafayette Indiana 47905
GSK Clinical Trials Call Center Cedar Rapids Iowa 52401
GSK Clinical Trials Call Center Overland Park Kansas 66211
GSK Clinical Trials Call Center Baltimore Maryland 21204
GSK Clinical Trials Call Center Rockville Maryland 20852
GSK Clinical Trials Call Center Belmont Massachusetts 02478
GSK Clinical Trials Call Center Detroit Michigan 48207
GSK Clinical Trials Call Center Farmington Hills Michigan 48334
GSK Clinical Trials Call Center Minneapolis Minnesota 55454
GSK Clinical Trials Call Center St Louis Missouri 63108
GSK Clinical Trials Call Center Omaha Nebraska 68198
GSK Clinical Trials Call Center Clementon New Jersey 08021
GSK Clinical Trials Call Center Kenilworth New Jersey 07033
GSK Clinical Trials Call Center Princeton New Jersey 08540
GSK Clinical Trials Call Center Albany New York 12208
GSK Clinical Trials Call Center New York New York 10021
GSK Clinical Trials Call Center New York New York 10024
GSK Clinical Trials Call Center New York New York 10025
GSK Clinical Trials Call Center Rochester New York 14618
GSK Clinical Trials Call Center Beachwood Ohio 44122
GSK Clinical Trials Call Center Cincinnati Ohio 45267
GSK Clinical Trials Call Center Dayton Ohio 45415
GSK Clinical Trials Call Center Marion Ohio 43302
GSK Clinical Trials Call Center Eugene Oregon 97401
GSK Clinical Trials Call Center Portland Oregon 97210
GSK Clinical Trials Call Center Portland Oregon 97239
GSK Clinical Trials Call Center Havertown Pennsylvania 19083
GSK Clinical Trials Call Center Jenkintown Pennsylvania 19046
GSK Clinical Trials Call Center Philadelphia Pennsylvania 19131
GSK Clinical Trials Call Center East Providence Rhode Island 02915
GSK Clinical Trials Call Center Woodstock Vermont 05091
GSK Clinical Trials Call Center Falls Church Virginia 22041
GSK Clinical Trials Call Center Bellevue Washington 98004
GSK Clinical Trials Call Center Seattle Washington 98105
GSK Clinical Trials Call Center Spokane Washington 99204
GSK Clinical Trials Call Center 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.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 8 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00046241, 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 Jan 22, 2017 · Synced Jul 23, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00046241 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →