Last updated: 11/07/2018 20:00:14

Prospective open evaluation of the seizure incidence with bupropion hydrochloride (Wellbutrin®)

GSK study ID
Well 86A
Clinicaltrials.gov ID
Not applicable
EudraCT ID
Not applicable
EU CT Number
Not applicable
Trial status
Study complete
Study complete
Overview
Eligibility
Locations
Study documents
Results summary
Plain language summaries
Additional information

Trial overview

Official title: Prospective open evaluation of the seizure incidence with bupropion hydrochloride (Wellbutrin®)
Trial description: Prospective open evaluation of the seizure incidence with bupropion hydrochloride (Wellbutrin®)
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:
Johnston JA, Lineberry CG, Ascher, JA, et.al. A 102-Center Prospective Study of Seizure in Association with Bupropion. J Clin Psychiatry 1991;52:450-456.
Medical condition
Depressive Disorder, Major
Product
bupropion
Collaborators
Not applicable
Study date(s)
N/A to Invalid Date
Type
Not applicable
Phase
4

Participation criteria

Sex
Not applicable
Age
Not applicable
Accepts healthy volunteers
Not applicable

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

Not applicable

Recruitment status
Study complete
Actual primary completion date
Not applicable
Actual study completion date
Not applicable

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

Not applicable
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