Last updated: 11/07/2018 13:53:29
A Double-Blind Comparison of the Efficacy and Tolerability of Paroxetine and Imipiramine in the Treatment of Depression and Behavioural Disturbance Associated with Dementia
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 Comparison of the Efficacy and Tolerability of Paroxetine and Imipiramine in the Treatment of Depression and Behavioural Disturbance Associated with Dementia
Trial description: A Double-Blind Comparison of the Efficacy and Tolerability of Paroxetine and Imipiramine in the Treatment of Depression and Behavioural Disturbance Associated with Dementia
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:
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Interventions:
Not applicable
Enrollment:
Not applicable
Primary completion date:
Not applicable
Observational study model:
Not applicable
Time perspective:
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Clinical publications:
A double-blind comparison of the efficacy and safety of paroxetine and imipramine in the treatment of depression with dementia. Hunter, B and Judge, R International Academy for Biomedical and Drug Research 1996 Campaign on Interface Between Psychiatry and Internal Medicine Workshop on New Therapeutic Indications of Antidepressants 3/22/1996 Brugge; Belgium
A double-blind comparison of the efficacy and safety of paroxetine and imipramine in the treatment of depression with dementia. Hunter, B and judge, R 8th Congress of the Association of European Psychiatrists/Annual Meeting of the Royal College of Psychiatrists 7/7/1996 London; UK
A double-blind comparison of the efficacy and safety of paroxetine and imipramine in the treatment of depression with dementia. Le Katona, C, Hunter, B, and Judge, R 10th World Congress of Psychiatry 8/23/1996 Madrid; Spain
Katona et al. A double-blind comparison of the efficacy and safety of paroxetine and imipramine in the treatment of depression with dementia. Int. J. Geriatric Psychiatry 1998; 13:100-108.
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
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Recruitment status
Study complete
Actual primary completion date
Not applicable
Actual study completion date
1995-10-02
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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