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Clinical Trials/IRCT20190204042618N3
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

Esfahan University of Medical Sciences0 sites200 target enrollmentTBD

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.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
7 years ago
Study Type
Interventional
Sex
Female

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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