Decreasing the Incidence of Post-Operative Nausea and Vomiting (PONV) in Bariatric Patients
Completed · Not applicable · Has a placebo group
Conditions studied: Nausea, Vomiting
In brief
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.
Key facts
- Study ID
- NCT00956215
- Run by
- University of Pennsylvania
- People needed
- 125
- Starts
- 2010-05-01
- Expected to finish
- 2012-01-01
- Last updated by the study team
- 2012-02-16
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Subjects included in this study must be:
- Female
- At least 18 years of age
- Non-smoking
- At high risk for PONV
- Obese with a BMI of at least 45 kg/m2
- Undergoing upper gastrointestinal surgery requiring postoperative opioid analgesia
You may not qualify if…
- Subjects will be excluded if:
- They have a known allergy to Aprepitant or Ondansetron
- They are currently taking Orap (pimozide), Seldane (terfenadine), Hismanal (astemizole), or Propulsid (cisapride)
- They are pregnant
- They are breastfeeding
- They plan on getting pregnant in the 2 months following surgery
- They are not able to receive patient controlled analgesia (PCA) following surgery
- They have a known drug or alcohol abuse problem
- They have chronic nausea and vomiting
Where it is running
- University of Pennsylvania — Philadelphia, Pennsylvania, United States
Full record on ClinicalTrials.gov
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