Clinical Trials Directory

Trials / Completed

CompletedNCT00452855

Sevoflurane-Remifentanil Anaesthesia. The Risk of Post Operative Nausea

Postoperative Nausea and Vomiting Are Similar When Propofol or Sevoflurane Are Used as Adjuvant to Remifentanil During Anaesthesia for Gynaecological Surgery

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
160 (planned)
Sponsor
Central Jutland Regional Hospital · Academic / Other
Sex
Female
Age
18 Years – 50 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to determine whether sevoflurane-remifentanil anaesthesia is similar to propofol-remifentanil anaesthesia concerning post- operative nausea and vomiting.

Detailed description

Propofol and sevoflurane anaesthesia are used world wide at the anaesthetists discretion. Propofol is superior to inhalational anaesthetics as anaesthesia for patients at risk of post operative nausea and vomiting (PONV) as PONV is diminished. However, when remifentanil is used as adjuvant to sevoflurane, the total dose of the latter is reduced. Therefore, we wanted to investigate if sevoflurane-remifentanil anaesthesia is similar to propofol-remifentanil anaesthesia with emphasis on nausea, vomiting and total PONV during 24 hours. In the post anaesthesia care unit (PACU) and in the surgical ward nausea was scored on a visual analogue score. Vomiting was registered.

Conditions

Interventions

TypeNameDescription
PROCEDURESevoflurane-remifentanil anaesthesia

Timeline

Start date
2002-01-01
Completion
2005-05-01
First posted
2007-03-28
Last updated
2007-03-29

Locations

1 site across 1 country: Denmark

Source: ClinicalTrials.gov record NCT00452855. Inclusion in this directory is not an endorsement.