Trials / Withdrawn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- Withdrawn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
| Type | Name | Description |
|---|---|---|
| DRUG | aprepitant | Emend 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.