Last updated: 11/07/2018 13:50:58
A study to assess the CNS effects of paroxetine, and haloperidol and any interaction of paroxetine with the sedative effects of haloperidol
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 study to assess the CNS effects of paroxetine, and haloperidol and any interaction of paroxetine with the sedative effects of haloperidol
Trial description: A study to assess the CNS effects of paroxetine, and haloperidol and any interaction of paroxetine with the sedative effects of haloperidol
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:
The psychomotor effects of paroxetine alone and in combination with haloperidol, amylobarbitone, oxazepam, or alcohol. Cooper, S. M., Jackson, D., Loudon, J. M., McClelland, G. R., and Raptopoulos, P. Acta Psychiatr Scand Suppl 89; 350(53-5)
Medical condition
Mental Disorders
Product
paroxetine
Collaborators
Not applicable
Study date(s)
January 1984 to January 1984
Type
Not applicable
Phase
1
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
Not applicable
Recruitment status
Study complete
Actual primary completion date
Not applicable
Actual study completion date
1984-29-01
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
Not applicable
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