IRCT20190204042618N3
Completed
Phase 3
Comparing the efficacy of standard spinal anesthesia and transversus abdominis plane block with Ropivacaine 0.5% on relieving the postoperative pain after laparoscopic gynecologic surgery
Overview
- Phase
- Phase 3
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Esfahan University of Medical Sciences
- Enrollment
- 200
- Status
- Completed
- Last Updated
- 7 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
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
Outcomes
Primary Outcomes
Not specified
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