Clinical Trials Directory

Trials / Completed

CompletedNCT01020903

Aprepitant for Post-operative Nausea

Aprepitant vs. Placebo for the Prevention of Postoperative Nausea and Vomiting: a Randomized, Double-blind Study in Patients Undergoing Laparoscopic Cholecystectomy

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
200 (actual)
Sponsor
Northwell Health · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Anesthesia, especially for laparoscopic surgery, can cause post-operative nausea and vomiting. Most patients are given two drugs, decadron and ondansetron, to try to minimize this. This study is to determine if a new drug, aprepitant, would add any benefit in terms of post-op nausea prevention. All laparoscopic cholecystectomy study patients will receive decadron and ondansetron. Half the patients will receive aprepitant in addition. The other half will receive placebo. The study will be randomized and double-blind.

Conditions

Interventions

TypeNameDescription
PROCEDUREAprepitant40 mg po pre-op
DRUGPlaceboOrally, pre-op

Timeline

Start date
2009-11-01
Primary completion
2010-11-01
Completion
2010-11-01
First posted
2009-11-26
Last updated
2023-11-22
Results posted
2015-06-04

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01020903. Inclusion in this directory is not an endorsement.