Trials / Completed
CompletedNCT05759481
Prevention of Post-Operative Nausea and Vomiting With Propofol Infusion
- Status
- Completed
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 68 (actual)
- Sponsor
- Milton S. Hershey Medical Center · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to clarify whether or not a low-dose propofol infusion can effectively prevent postoperative nausea and vomiting (PONV) in patients who have a documented history of PONV and/or motion sickness.
Detailed description
Propofol is administered as both low dose and as sole anesthetic in patients with history of PONV and/or motion sickness. But efficacy of one dose over the other is not studied. This study plans to clarify if propofol in low dose is as effective as its administration as sole anesthetic in patients with history of PONV and/or motion sickness
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Propofol | Propofol is administered starting at surgery induction and ending at skin closure |
| OTHER | Placebo | Placebo is administered starting at surgery induction and ending at skin closure |
Timeline
- Start date
- 2024-02-01
- Primary completion
- 2025-03-12
- Completion
- 2025-03-12
- First posted
- 2023-03-08
- Last updated
- 2025-04-02
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated drug study
Source: ClinicalTrials.gov record NCT05759481. Inclusion in this directory is not an endorsement.