Last updated: 11/07/2018 18:28:56
A Randomized, Double-Blind, Placebo-Controlled Study of Intravenous Ondansetron Versus Droperidol for the Prevention of Postoperative Nausea and Vomiting in Outpatient Surgery
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 Randomized, Double-Blind, Placebo-Controlled Study of Intravenous Ondansetron Versus Droperidol for the Prevention of Postoperative Nausea and Vomiting in Outpatient Surgery
Trial description: A Randomized, Double-Blind, Placebo-Controlled Study of Intravenous Ondansetron Versus Droperidol for the Prevention of Postoperative Nausea and Vomiting in Outpatient Surgery
Primary purpose:
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Trial design:
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Masking:
Not applicable
Allocation:
Not applicable
Primary outcomes:
Not applicable
Secondary outcomes:
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Interventions:
Not applicable
Enrollment:
Not applicable
Primary completion date:
Not applicable
Observational study model:
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Time perspective:
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Clinical publications:
Fortney J, Graczyk S, Creed M, Gan TJ. S3A-409/410 Study Group. A comparison of ondansetron and droperidol as prophylactic antiemetic therapy for elective outpatient surgical procedures. Anesthesiology 1997;87(3A):A21 (abstract)
Fortney JT, Gan TJ, Graczyk S, et al. A comparison of the efficacy, safety, and patient satisfaction of ondansetron versus droperidol as antiemetics for elective outpatient surgery. Anesth Analg 1998;86:731-38.
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
1994-30-12
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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