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
| Type | Name | Description |
|---|---|---|
| DRUG | Aprepitant | 80 mg tablet of Aprepitant with 50 ml of water 30 minutes before surgery |
| DRUG | Aprepitant placebo | 80 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.