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Prevention of Intraoperative Nausea and Vomiting During Cesarean Section

NCT01216410 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 306

Last updated 2014-08-06

Study results available
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Summary

The study investigates the incidence of intraoperative nausea and vomiting under spinal anesthesia using a phenylephrine infusion with and without prophylactic antiemetics.

Conditions

  • Cesarean Delivery

Interventions

DRUG

Metoclopramide

Prophylactic Metoclopramide 10 mg given before spinal together with prophylactic phenylephrine infusion

DRUG

Phenylephrine infusion

Prophylactic phenylephrine infusion after spinal and placebo antiemetics

DRUG

Combination Group

Metoclopramide and ondansetron prophylaxis with phenylephrine infusion

Sponsors & Collaborators

Study Design

Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
45 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-12-31
Primary Completion
2011-04-30
Completion
2011-04-30

Countries

  • United States

Study Locations

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Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01216410 on ClinicalTrials.gov