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Prevention of Seasonal Affective Disorder

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00046449
Enrollment
Unknown
Registered
2002-10-02
Start date
2002-09-30
Completion date
2003-06-30
Last updated
2015-06-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Seasonal Affective Disorder (SAD)

Brief summary

A Placebo Controlled Study Evaluating The Effectivess Of Medication In Preventing Seasonal Affective Disorder

Interventions

DRUGInvestigational Seasonal Affective Disorder (SAD) Drug

Sponsors

GlaxoSmithKline
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

(Patient must meet these criteria in order to be eligible for this study.) * Patient has a history of Major Depressive Disorder (MDD) with a seasonal pattern.

Exclusion criteria

(Patient cannot meet these criteria in order to be eligible for this study.) * Patient has a current or past history of seizure disorder or brain injury. * Patient has a history or current diagnosis of anorexia nervousa 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.

Countries

Canada, United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026