Prevention of Seasonal Affective Disorder

NCT ID: NCT00046241

Last Updated: 2017-01-23

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE3

Total Enrollment

300 participants

Study Classification

INTERVENTIONAL

Study Start Date

2002-09-30

Study Completion Date

2003-06-30

Brief Summary

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This is a placebo controlled study evaluating the effectiveness of medication in preventing depressive episodes in subjects with a history of Seasonal Affective Disorder (SAD).

Detailed Description

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Conditions

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Seasonal Affective Disorder

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Interventions

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Extended-release bupropion hydrochloride

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* Patient has a history of Major Depressive Disorder (MDD) with a seasonal pattern.

Exclusion Criteria

* Patient has a current or past history of seizure disorder or brain injury.
* Patient has a history or current diagnosis of anorexia nervosa or bulimia.
* Patient has recurrent summer depression more frequently than winter depression.
* Patient has primary diagnosis of panic disorder, Obsessive Compulsive Disorder (OCD), Posttraumatic Stress Disorder (PTSD), acute distress disorder, bipolar II disorder or other psychotic disorders.
* Patient has initiated psychotherapy within the last 3 months.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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GlaxoSmithKline

INDUSTRY

Sponsor Role lead

Principal Investigators

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GSK Clinical Trial, MD

Role: STUDY_DIRECTOR

GlaxoSmithKline

Locations

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GSK Clinical Trials Call Center

Anchorage, Alaska, United States

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Hamden, Connecticut, United States

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Boise, Idaho, United States

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Chicago, Illinois, United States

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Edwardsville, Illinois, United States

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Oak Brook, Illinois, United States

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Oakbrook Terrace, Illinois, United States

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Lafayette, Indiana, United States

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Cedar Rapids, Iowa, United States

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Overland Park, Kansas, United States

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Baltimore, Maryland, United States

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Rockville, Maryland, United States

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Belmont, Massachusetts, United States

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Detroit, Michigan, United States

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Farmington Hills, Michigan, United States

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Minneapolis, Minnesota, United States

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St Louis, Missouri, United States

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Omaha, Nebraska, United States

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Clementon, New Jersey, United States

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Kenilworth, New Jersey, United States

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Princeton, New Jersey, United States

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Albany, New York, United States

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New York, New York, United States

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New York, New York, United States

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New York, New York, United States

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Rochester, New York, United States

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Beachwood, Ohio, United States

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Cincinnati, Ohio, United States

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Dayton, Ohio, United States

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Marion, Ohio, United States

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Eugene, Oregon, United States

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Portland, Oregon, United States

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Portland, Oregon, United States

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Havertown, Pennsylvania, United States

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Jenkintown, Pennsylvania, United States

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Philadelphia, Pennsylvania, United States

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East Providence, Rhode Island, United States

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Woodstock, Vermont, United States

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Falls Church, Virginia, United States

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Bellevue, Washington, United States

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Seattle, Washington, United States

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Spokane, Washington, United States

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Brown Deer, Wisconsin, United States

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Calgary, Alberta, Canada

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Edmonton, Alberta, Canada

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Kelowna, British Columbia, Canada

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Winnipeg, Manitoba, Canada

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Toronto, Ontario, Canada

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Toronto, Ontario, Canada

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Montreal, Quebec, Canada

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GSK Clinical Trials Call Center

Sherbrooke, Quebec, Canada

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Countries

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United States Canada

Other Identifiers

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AK130930

Identifier Type: -

Identifier Source: org_study_id

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