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Prevention Post Operative Nausea Vomiting in Ambulatory Gynecologic Laparoscopy

Information source: Prince of Songkla University
ClinicalTrials.gov processed this data on August 20, 2015
Link to the current ClinicalTrials.gov record.

Condition(s) targeted: Postoperative Nausea and Vomiting

Intervention: Dexamethasone (Drug); Ondansetron (Drug); Dimenhydrinate (Drug)

Phase: Phase 2

Status: Completed

Sponsored by: Prince of Songkla University

Official(s) and/or principal investigator(s):
Thanyamon Asampinwat, MD, Principal Investigator, Affiliation: Anesthesiology department, Faculty of Medicine, Prince of Songkla University Thailand


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.

Clinical Details

Study design: Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Treatment

Primary outcome: Incidence of PONV in ambulatory gynecologic laparoscopy


Minimum age: 18 Years. Maximum age: 45 Years. Gender(s): Female.


Inclusion Criteria:

- Ambulatory gynecologic laparoscopy

- Age 18-45 years

- ASA class 1-2

Exclusion Criteria:

- The patients who take opioid, steroid, pyschotics or antiemetic drug within 24 hours

before surgery

- History of antiemetic, anesthetic and analgesic drugs allergy

- Pregnancy or breast feeding

- Body mass index >34 kg/square metre

Locations and Contacts

Anesthesiology Department, Faculty of Medicine, Prince of Songkla University, Hat Yai, Songkhla 90110, Thailand
Additional Information

Starting date: March 2008
Last updated: July 29, 2012

Page last updated: August 20, 2015

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