Last updated: 03/17/2021 08:30:18
A multi-centre study to assess the effectiveness and tolerance of paroxetine by double-blind comparison with amitriptyline
Clinicaltrials.gov ID
Not applicable
EudraCT ID
Not applicable
EU CT Number
Not applicable
Trial status
Study complete
Study complete
Trial overview
Official title: A multi-centre study to assess the effectiveness and tolerance of paroxetine by double-blind comparison with amitriptyline
Trial description: A multi-centre study to assess the effectiveness and tolerance of paroxetine by double-blind comparison with amitriptyline
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:
Cardiovascular effects of paroxetine. Kuhs, H. and Rudolf, G. A. Psychopharmacology (Berl) 90; 102(3):379-82
Kuhs H et al. A double-blind study of paroxetine versus amitriptyline, with particular reference to cardiovascular effects. Proceedings of the World Congress of Biological Psychiatry 1991: 22-23 (poster presentation)
Relationship between parameters of serotonin transport and antidepressant plasma levels or therapeutic response in depressive patients treated with paroxetine and amitriptyline. Kuhs, H., Schlake, H. P., Rolf, L. H., and Rudolf, G. A. Acta Psychiatr Scand 92; 85(5):364-9
Medical condition
Depressive Disorder, Major
Product
paroxetine
Collaborators
Not applicable
Study date(s)
N/A to Invalid Date
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
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
Additional information
Not applicable
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Access to clinical trial data by researchers
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