The effect of transversus abdominis plane block with Ropivacaine on postoperative pai
Phase 3
- Conditions
- Pain after laparoscopic gynecologic surgery.
- Registration Number
- IRCT20190204042618N3
- Lead Sponsor
- Esfahan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 200
Inclusion Criteria
Candidate for laparoscopic gynecologic surgery (such as ovarian cystectomy and hysterectomy)
Willingness to participate in the study
Exclusion Criteria
Having a history of allergy to the agents used in the study
suffering from acute and/or chronic preoperative pains
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Severity of pain. Timepoint: At the time of recovery, 30 minutes, 2, 4, 6, 12, and 48 hours after surgery. Method of measurement: VAS (Visual analogue scale).;Severity of nausea and vomiting. Timepoint: At the time of recovery, 30 minutes, 2, 4, 6, 12, and 48 hours after surgery. Method of measurement: Based on questionnaire and its scoring (0 = no nausea and vomiting, 1 = mild, 2 = moderate and 3 = severe).
- Secondary Outcome Measures
Name Time Method