Comparison of intraoperative opioid use in two opioid injections by Analgesia nociception index (ANI) and conventional method
Phase 2
Recruiting
- Conditions
- Pain.Pain, not elsewhere classified
- Registration Number
- IRCT20120814010599N30
- Lead Sponsor
- Iran University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 90
Inclusion Criteria
Candidate of laparoscopic gynecological surgery
Age between 18-45 years
Body mass index (BMI) less than 25
Exclusion Criteria
Having cardiac arrhythmia
Patients with central or autonomic neurological problems undergoing opioid treatment
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Total dose of opioid used during surgery. Timepoint: After surgery. Method of measurement: Patient file.
- Secondary Outcome Measures
Name Time Method Pain. Timepoint: At 1, 12 and 24 hours after surgery. Method of measurement: Visual analog scale.