Propofol and remifentanil requirements after acute ethanol intake in clinical settings

Completed

• Conditions: Interaction of acute ethanol intravenous intake with propofol (general anesthetic) and remifentanil (opioid); Surgery; Anaesthesia

• Registration Number: ISRCTN73421343
• Lead Sponsor: Theagenio Anticancer Hospital of Thessaloniki (Greece)

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2005-07-08
• Last Update Posted: 13 January 2015

Recruitment & Eligibility

• Status: Completed
• Sex: Female
• Target Recruitment: 60

Inclusion Criteria

Female surgical patients on general anesthesia

Exclusion Criteria

Alcoholic patients, patients in abstinence

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Reduction of propofol and remifentanil requirements

Secondary Outcome Measures

Name	Time	Method
Degree of reduction, side-effects