Evaluation of quality of recovery after general anesthesia with isoflurane compared with propofol in abdominal hysterectomy

Phase 3

Recruiting

• Conditions: Quality of recovery in abdominal hysterectomy.; Other complications of anesthesia; T88.59

• Registration Number: IRCT20110409006148N5
• Lead Sponsor: Babol University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 17 August 2020

Recruitment & Eligibility

• Status: Recruiting
• Sex: Female
• Target Recruitment: 80

Inclusion Criteria

80 female patients 30 to 65 years old with 1 and 2 stages of health based on American Society of Anesthesiologists(ASA) who are candidates for abdominal hysterectomy

Exclusion Criteria

Body Mass Index more than 30 kg/m2
Difficult airway
Psychotic disorders

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Quality of recovery. Timepoint: 24 hours before surgery-24 hours after surgery-48 hours after surgery. Method of measurement: Questionnaire of quality of recovery-15.;Post operative pain. Timepoint: 24 hours before surgery-24 hours after surgery-48 hours after surgery. Method of measurement: Questionnaire of quality of recovery-15.;Nausea and vomiting. Timepoint: 24 hours before surgery-24 hours after surgery-48 hours after surgery. Method of measurement: Questionnaire of quality of recovery-15.