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Prevention Post Operative Nausea Vomiting in Ambulatory Gynecologic Laparoscopy

NCT01543945 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 340

Last updated 2012-07-31

No results posted yet for this study

Summary

The purpose of this study is to compare the incidence of Postoperative nausea and vomiting between the intervention group who received multimodal antiemetic management and the control group who did not get this protocol.

Conditions

  • Postoperative Nausea and Vomiting

Interventions

DRUG

Dexamethasone

4 mg iv before induction for high and extremely high risk

DRUG

Ondansetron

4 mg iv before ended surgery 30 min

DRUG

Dimenhydrinate

1 mg/kg iv before ended surgery 30 min

Sponsors & Collaborators

  • Prince of Songkla University

    lead OTHER

Principal Investigators

  • Thanyamon Asampinwat, MD · Anesthesiology department, Faculty of Medicine, Prince of Songkla University Thailand

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

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

Timeline & Regulatory

Start
2008-03-31
Primary Completion
2011-12-31

Countries

  • Thailand

Study Locations

More Related Trials

Entities

Drugs

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 NCT01543945 on ClinicalTrials.gov