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NCT00659737 · ClinicalTrials.gov registry record · NA
Comparison of Oral Aprepitant and Transdermal Scopolamine for Preventing Postoperative Nausea and Vomiting
A NA study, sponsored by Drexel University College of Medicine.
- Completed
- Registry status
- NA
- Development phase
- 115
- Enrollment target
NCT00659737: Completed NA study, sponsored by Drexel University College of Medicine.
NCT00659737 is a NA study that has completed, run by Drexel University College of Medicine. The registered enrollment target is 115 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (92% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00659737, a NA study, has completed, sponsored by Drexel University College of Medicine.
- COMPLETED
- Registry status
- NA
- Development phase
- 115 participants
- Enrollment target
Study 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.
Interventions
- DRUG Scopolamine
- DRUG Aprepitant
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 115 participants |
| Start Date | 2008-04 |
| Est. Completion | 2010-03 |
| Phase | NA |
What the finished NCT00659737 record still lists
NCT00659737 is an interventional study that assigns participants to a tested intervention. The registered 115 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (92% lower).
The record links to 0 conditions, and to 2 interventions - of which Scopolamine is the first listed.
NCT00659737 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00659737 about?
NCT00659737 is a clinical study titled "Comparison of Oral Aprepitant and Transdermal Scopolamine for Preventing Postoperative Nausea and Vomiting". 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 transd...
What is the current status of trial NCT00659737?
This trial is currently completed. It is a NA study. The enrollment target is 115 participants. The study started on 2008-04. Estimated completion is 2010-03.
What interventions are being tested in trial NCT00659737?
The interventions under investigation include: Scopolamine (DRUG), Aprepitant (DRUG).
Who is sponsoring clinical trial NCT00659737?
This trial is sponsored by Drexel University College of Medicine, which has 25 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00659737's enrollment target sits among peer trials
115 810th of 2000 higher than 1,190 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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