Clinical Trials Directory

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

TypeNameDescription
DRUGPropofolPropofol is administered starting at surgery induction and ending at skin closure
OTHERPlaceboPlacebo 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

Source: ClinicalTrials.gov record NCT05759481. Inclusion in this directory is not an endorsement.