Last updated: 04/13/2020 16:50:19
Six-week, parallel, double-blind, randomized comparison of bupropion and trazodone (150-400mg/day) in outpatients – Extensive searching has revealed that no clinical study report is available for this study. The clinical trial results were reported via publication; see citations below.
Clinicaltrials.gov ID
Not applicable
EudraCT ID
Not applicable
EU CT Number
Not applicable
Trial status
Study complete
Study complete
Trial overview
Official title: Six-week, parallel, double-blind, randomized comparison of bupropion and trazodone (150-400mg/day) in outpatients – Extensive searching has revealed that no clinical study report is available for this study. The clinical trial results were reported via publication; see citations below.
Trial description: Six-week, parallel, double-blind, randomized comparison of bupropion and trazodone (150-400mg/day) in outpatients – Extensive searching has revealed that no clinical study report is available for this study. The clinical trial results were reported via publication; see citations below.
Primary purpose:
Not applicable
Trial design:
Not applicable
Masking:
Not applicable
Allocation:
Not applicable
Primary outcomes:
Not applicable
Secondary outcomes:
Not applicable
Interventions:
Not applicable
Enrollment:
Not applicable
Primary completion date:
Not applicable
Observational study model:
Not applicable
Time perspective:
Not applicable
Clinical publications:
Segraves RT, Clayton ALH, Croft HA, Wolf A. Multicenter Study of Bupropion in Female Hypoactive Sexual Desire Disorder Supported by GlaxoSmithKline 156th Annual Meeting of the American Psychiatric Association 5/17/2003 San Francisco, California.
Weisler RH, Johnston JA, Lineberry CG, Samara B, Branconnier RJ. Comparison of Bupropion and Trazodone for the Treatment of Major Depression - (J Clin Psychopharmacol 1994;14:170-179).
Medical condition
Depressive Disorder
Product
Not applicable
Collaborators
Not applicable
Study date(s)
January 1991 to January 1991
Type
Interventional
Phase
3
Participation criteria
Sex
Not applicable
Age
Not applicable
Accepts healthy volunteers
Not applicable
Inclusion and exclusion criteria
Trial location(s)
This study does not involve prospective enrollment of participants.
Study documents
Scientific result summary
Available language(s): English
If you wish to request for full study report, please contact - [email protected]
Results overview
Refer to study documents
Recruitment status
Study complete
Actual primary completion date
Not applicable
Actual study completion date
1991-01-01
Plain language summaries
Plain language summaries of clinical trial results for Phase 2-4 clinical trials that were initiated on or after January 2022 will be posted by GSK within one year following study completion.
Additional information about the trial
Additional information
Not applicable
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