Patients´ recovery day 0-3 after short-stay elective surgery – a pilot study comparing desflurane and propofol TCI as main anaesthetics. - Cognitive functio

Phase 1

• Conditions: Patients undergoing elective general anaesthesia for breat surgery; MedDRA version: 12.1Level: LLTClassification code 10002091Term: Anaesthesia

• Registration Number: EUCTR2011-000922-31-SE
• Lead Sponsor: Karolinska Institutet

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2011-03-02
• Study Completion: 2013-05-30
• Last Update Posted: 19 April 2022

Recruitment & Eligibility

• Status: ot Recruiting
• Sex: Female
• Target Recruitment: 60

Inclusion Criteria

ASA 1-2 females scheduled for elective breast surgery under general anaesthesia with an estimated surgical duration of 60-90 minutes
Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range
F.1.3 Elderly (>=65 years) no
F.1.3.1 Number of subjects for this age range

Exclusion Criteria

Any cognitive or psychiatric difficiency
Uncontrolled, cardiovascular, hepatic or renal disease.

Study & Design

• Study Type: Interventional clinical trial of medicinal product
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Main Objective: Study recovery, resumption of cognitive capacity after end of anaesthesia;Secondary Objective: Study variability in time taken to regain cognitive capacity;Primary end point(s): Postoperative Recovery Scale score at 24 hours