Last updated: 11/07/2018 13:44:50
A Controlled Double-blind Randomised Parallel Group Study Comparing the Effects of Paroxetine and Maprotiline in the Treatment of Out-Patients with Major and Minor Depression
Clinicaltrials.gov ID
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EudraCT ID
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EU CT Number
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Trial status
Study complete
Study complete
Trial overview
Official title: A Controlled Double-blind Randomised Parallel Group Study Comparing the Effects of Paroxetine and Maprotiline in the Treatment of Out-Patients with Major and Minor Depression
Trial description: A Controlled Double-blind Randomised Parallel Group Study Comparing the Effects of Paroxetine and Maprotiline in the Treatment of Out-Patients with Major and Minor Depression
Primary purpose:
Not applicable
Trial design:
Not applicable
Masking:
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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:
A double-blind study comparing paroxetine and maprotiline in depressed outpatients. Szegedi, A., Wetzel, H., Angersbach, D., Dunbar, G. C., Schwarze, H., Philipp, M., and Benkert, O. Pharmacopsychiatry 97; 30(3):97-105
Szegedi et al. Response to treatment in minor and major depression: results of a double-blind comparative study with paroxetine and maprotiline. J. Affective Disord 1997; 45:167-178
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
Not applicable
Recruitment status
Study complete
Actual primary completion date
Not applicable
Actual study completion date
1992-21-10
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
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