Last updated: 11/07/2018 18:23:48

Prevention of Postoperative Nausea and Vomiting: A Randomized, Double-blind Study of Intravenous Ondansetron in Female Patients Undergoing Laparoscopic Procedures.

GSK study ID
S3A-243
Clinicaltrials.gov ID
Not applicable
EudraCT ID
Not applicable
EU CT Number
Not applicable
Trial status
Study complete
Study complete
Overview
Eligibility
Locations
Study documents
Results summary
Plain language summaries
Additional information

Trial overview

Official title: Prevention of Postoperative Nausea and Vomiting: A Randomized, Double-blind Study of Intravenous Ondansetron in Female Patients Undergoing Laparoscopic Procedures.
Trial description: Prevention of Postoperative Nausea and Vomiting: A Randomized, Double-blind Study of Intravenous Ondansetron in Female Patients Undergoing Laparoscopic Procedures.
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:
Kovac A, McKenzie R, O’Connor T, Duncalf D, Angel J, Gratz I, Fagraeus I, McLeskey C, Joslyn A. Prophylactic intravenous ondansetron in female outpatients undergoing gynaecological surgery: a multicenter dose-comparison study. European Journal of Anaesthesiology – Supplement, November 1992;6:37-47.
McKenzie R, Kovac A, O’Connor T, Duncalf D, Angel J, Gratz I, Tolpin E, McLeskey C, Joslyn A. Comparison of ondansetron versus placebo to prevent postoperative nausea and vomiting in women undergoing ambulatory gynaecologic surgery. Anesthesiology 1993;78:21-28.
Medical condition
Nausea and Vomiting, Postoperative
Product
ondansetron
Collaborators
Not applicable
Study date(s)
November 1990 to June 1991
Type
Not applicable
Phase
2

Participation criteria

Sex
Not applicable
Age
Not applicable
Accepts healthy volunteers
Not applicable

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
1991-01-06

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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