Clinical Trials Directory

Trials / Completed

CompletedNCT00956215

Decreasing the Incidence of Post-Operative Nausea and Vomiting (PONV) in Bariatric Patients

A Randomized and Placebo-Controlled Evaluation of Aprepitant for Decreasing the Incidence of Post-Operative Nausea and Vomiting (PONV) in Bariatric Patients

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
125 (actual)
Sponsor
University of Pennsylvania · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The study drug, Aprepitant, is currently used to control chemotherapy induced nausea and vomiting and is also approved for post-operative nausea and vomiting. The investigators' evaluation of it in morbidly obese patients will demonstrate its ability to control nausea and vomiting post-operatively in this subset of patients.

Detailed description

The purpose of this study is to evaluate the effectiveness of Aprepitant, also known as Emend, in reducing post-operative nausea and vomiting in morbidly obese patients. Post-operative nausea and vomiting that occurs in morbidly obese patients can greatly increase the chances of complications during the post-operative period. By treating morbidly obese patients with Aprepitant, the goal is to reduce the risk of such complications that may be induced by nausea and vomiting.

Conditions

Interventions

TypeNameDescription
DRUGAprepitant80 mg tablet of Aprepitant with 50 ml of water 30 minutes before surgery
DRUGAprepitant placebo80 mg placebo tablet with 50 ml of water no later than 30 minutes before induction of anesthesia.

Timeline

Start date
2010-05-01
Primary completion
2012-01-01
Completion
2012-01-01
First posted
2009-08-11
Last updated
2012-02-16

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00956215. Inclusion in this directory is not an endorsement.