Clinical Trials Directory

Trials / Completed

CompletedNCT00659737

Comparison of Oral Aprepitant and Transdermal Scopolamine for Preventing Postoperative Nausea and Vomiting

A Randomized, Double-blind Comparison of Oral Aprepitant Alone Versus Oral Aprepitant and Transdermal Scopolamine for Preventing Postoperative Nausea and Vomiting

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
115 (actual)
Sponsor
Drexel University College of Medicine · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Not accepted

Summary

Recent evidence suggests multiple drug therapy is superior to single agents. The study compares the incidence of nausea, vomiting, need for rescue medication, prolonged PACU time, and unplanned hospital admission in patients with high risk for PONV treated with oral aprepitant with or without transdermal scopolamine preoperatively.

Detailed description

Postoperative nausea and vomiting (PONV) is a serious problem complicating surgery. PONV has an overall incidence of 30% and a 70% incidence in high-risk patients. PONV yields unplanned hospital admission, pulmonary aspiration, esophageal rupture, electrolyte abnormalities, dehydration, and delayed discharge from the postanesthesia care unit (PACU). Additional use of resources costs the health care industry hundreds of millions of dollars annually. Patient satisfaction is greatly improved when PONV is prevented.4 PONV etiology is multifactorial and the treatment is multimodal.

Conditions

Interventions

TypeNameDescription
DRUGAprepitant40mg tablet
DRUGScopolamine1.5 mg patch delivering transdermally in vivo approx. 1.0mg over 3 days

Timeline

Start date
2008-04-01
Primary completion
2010-03-01
Completion
2010-03-01
First posted
2008-04-16
Last updated
2014-05-15
Results posted
2014-04-29

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00659737. Inclusion in this directory is not an endorsement.