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Completed

NCT Number: NCT01543945

Prevention Post Operative Nausea Vomiting in Ambulatory Gynecologic Laparoscopy

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.

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Key information

Age range

18 year–45 year

Sex eligibility

Female

Study type

Interventional

Phase

Phase 2

Primary location

Anesthesiology Department, Faculty of Medicine, Prince of Songkla University

Hat Yai, Changwat Songkhla, 90110, Thailand

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Dexamethasone

Drug

4 mg iv before induction for high and extremely high risk

Other names: Multimodal antiemetic group :, high risk : dexamethasone 4 mg + ondansetron 4 mg, Extremely high risk : dexamethasone 4 mg +, ondansetron 4 mg +, dimenhydrinate 1 mg

ondansetron

Drug

4 mg iv before ended surgery 30 min

Dimenhydrinate

Drug

1 mg/kg iv before ended surgery 30 min

Primary outcomes

  1. Incidence of PONV in ambulatory gynecologic laparoscopy

    Time frame: four year

Sponsors and collaborators

Lead sponsor

Prince of Songkla University

Other

Registry information

Important dates

Study start
2008
Primary completion
2011
First posted
Mar 5, 2012
Registry last updated
Jul 31, 2012

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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