Last updated: 11/07/2018 14:04:20
A double-blind, multicentre, parallel group study of paroxetine and amitriptyline in the treatment of patients with depression associated with breast cancer
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 double-blind, multicentre, parallel group study of paroxetine and amitriptyline in the treatment of patients with depression associated with breast cancer
Trial description: A double-blind, multicentre, parallel group study of paroxetine and amitriptyline in the treatment of patients with depression associated with breast cancer
Primary purpose:
Not applicable
Trial design:
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Masking:
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Allocation:
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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 comparative study of the effectiveness and tolerance of paroxetine and amitriptyline in treatment of breast cancer patients with clinically assessed depression: eine doppelblinde vergleichsstudie zur wirksamkeit und vertraglichkeit von paroxetin und amitriptylin bei der behandlung von brustkrebs-patientinnen mit klinisch nachgewiesener depression. Moslinger-Gehmayr, R., Zaninelli, R., Contu, A., Oberhoff, C., Gutschow, K., Schindler, A. E., and Staab, H. J. Zentralbl Gynakol 2000; 122(4):195-202
Depression in breast cancer patients - comparison of paroxetine and amitriptyline. A. Contu 10th Annual Congress of the European College of Neuropsychopharmacology (ECNP) 9/13/1997 Vienna; Austria
Depression in patients with breast cancer: a comparative study. Moslinger-Gehmayr, Regina 11th World Congress of Psychiatry (World Psychiatric Association) 8/6/1999 Hamburg; Germany
Pezzella et al. Treatment of depression in patients with breast cancer: a comparison between paroxetine vs amitriptyline. Breast Cancer Research and Treatment 2001; 70 (1): 1-10
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
1996-31-12
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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