Clinical Trials Directory

Trials / Withdrawn

WithdrawnNCT01186029

Comparison of Adding EMEND to PONV/PDNV Treatment Regimen

A Comparison Study to Determine the Increased Efficacy of Adding EMEND to the Treatment Regimen for Post-Discharge and Post-Operative Nausea and Vomiting

Status
Withdrawn
Phase
N/A
Study type
Interventional
Enrollment
0 (actual)
Sponsor
University of Nebraska · Academic / Other
Sex
All
Age
19 Years
Healthy volunteers
Not accepted

Summary

This study is looking at whether the addition of Aprepitant (Emend), an antiemetic, will provide added efficacy if added to 2 drugs that are already used as a standard of care for post-operative nausea and vomiting and post-discharge nausea and vomiting.

Detailed description

This study is looking at whether the addition of a fairly new drug for the treatment of post-operative nausea and vomiting (PONV) and post-discharge nausea and vomiting (PDNV) will provide added efficacy if added to 2 drugs that are already used as a standard of care for PONV and PDNV. The patients that will be looked at will be deemed at higher risk for PONV and PDNV based on the procedure they are having done and/or on patient risk factors.

Conditions

Interventions

TypeNameDescription
DRUGaprepitantEmend 40mg by mouth 30 minutes before procedure x 1

Timeline

Start date
2011-09-01
Primary completion
2011-09-01
Completion
2011-09-01
First posted
2010-08-20
Last updated
2024-08-30

Source: ClinicalTrials.gov record NCT01186029. Inclusion in this directory is not an endorsement.