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NCT01216410 · ClinicalTrials.gov registry record · NA
Prevention of Intraoperative Nausea and Vomiting During Cesarean Section
A NA study, sponsored by Duke University.
- Completed
- Registry status
- NA
- Development phase
- 306
- Enrollment target
NCT01216410: Completed NA study, sponsored by Duke University.
NCT01216410 is a NA study that has completed, run by Duke University. The registered enrollment target is 306 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (78% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01216410, a NA study, has completed, sponsored by Duke University.
- COMPLETED
- Registry status
- NA
- Development phase
- 306 participants
- Enrollment target
Study Summary
The study investigates the incidence of intraoperative nausea and vomiting under spinal anesthesia using a phenylephrine infusion with and without prophylactic antiemetics.
Primary Outcome
Comparison of intraoperative nausea and vomiting between the 3 groups.
Interventions
- DRUG Metoclopramide
- DRUG Phenylephrine infusion
- DRUG Combination Group
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 306 participants |
| Start Date | 2008-12 |
| Est. Completion | 2011-04 |
| Phase | NA |
What the finished NCT01216410 record still lists
NCT01216410 is an interventional study that assigns participants to a tested intervention. The registered 306 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 (78% lower).
The record links to 0 conditions, and to 3 interventions - of which Metoclopramide is the first listed.
NCT01216410 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01216410 about?
NCT01216410 is a clinical study titled "Prevention of Intraoperative Nausea and Vomiting During Cesarean Section". The study investigates the incidence of intraoperative nausea and vomiting under spinal anesthesia using a phenylephrine infusion with and without prophylactic antiemetics.
What is the current status of trial NCT01216410?
This trial is currently completed. It is a NA study. The enrollment target is 306 participants. The study started on 2008-12. Estimated completion is 2011-04.
What interventions are being tested in trial NCT01216410?
The interventions under investigation include: Metoclopramide (DRUG), Phenylephrine infusion (DRUG), Combination Group (DRUG).
Who is sponsoring clinical trial NCT01216410?
This trial is sponsored by Duke University, which has 1,725 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01216410's enrollment target sits among peer trials
306 324th of 2000 higher than 1,674 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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