Last updated: 11/19/2019 16:50:12
A Multicentre Double Blind Study Comparing Paroxetine at a Dose of 20mq Increasing to 30mg Taken in the Morning and Amitriptyline 75mg Increasing to 150mg in Divided Doses in Adult Patients with Major Depressive Disorder
Clinicaltrials.gov ID
Not applicable
EudraCT ID
Not applicable
EU CT Number
Not applicable
Trial status
Completed
Completed
Trial overview
Official title: A Multicentre Double Blind Study Comparing Paroxetine at a Dose of 20mq Increasing to 30mg Taken in the Morning and Amitriptyline 75mg Increasing to 150mg in Divided Doses in Adult Patients with Major Depressive Disorder
Trial description: A Multicentre Double Blind Study Comparing Paroxetine at a Dose of 20mq Increasing to 30mg Taken in the Morning and Amitriptyline 75mg Increasing to 150mg in Divided Doses in Adult Patients with Major Depressive Disorder
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
Observational study model:
Not applicable
Primary completion date:
1990-15-03
Time perspective:
Not applicable
Clinical publications:
Bignamini A et al. A double-blind multicenter study of paroxetine and amitriptyline in depressed outpatients. Int Clin Psychopharmacol 1992; 6(suppl 4): 37-42.
Inclusion and exclusion criteria
Trial location(s)
No location data available.
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
Completed
Actual primary completion date
1990-15-03
Actual study completion date
1990-15-03
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
Participate in clinical trial
Access to clinical trial data by researchers
Visit website