Evaluation of depth of anesthesia using two different methods in gynecologic laparoscopic surgery
Phase 2
- Conditions
- gynecologic surgery.Other complications of obstetric surgery and procedures
- Registration Number
- IRCT2015122919715N2
- Lead Sponsor
- Iran University of Medical Sciences, Vice Chancellor for Research
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 80
Inclusion Criteria
Age over 18 years; ASA class I-III; patients undergoing laparoscopic surgery for women; no history of chronic obstructive pulmonary disease; lack of kidney dysfunction; lack of neurologic disease; lack of addiction to opium or alcohol; not taking anticonvulsants and antidepressants; Lack of hypertension; lack of heart failure; patients with emergent surgery.
Exclusion criteria: Patients with difficult airway; Drug allergy.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Time of discharge from recovery. Timepoint: After the end of surgery. Method of measurement: Aldrete score.;Amount of used narcotics. Timepoint: Within the surgery. Method of measurement: Quantitative.;Pain. Timepoint: Within the surgery. Method of measurement: Visual analogue scale.
- Secondary Outcome Measures
Name Time Method