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Clinical Trials/IRCT20210302050553N1
IRCT20210302050553N1RecruitingPhase 3

Comparison of Ropivacaine combination with Dexamethasone analgesic effect and Ropivacaine combination with dexmedetomidine on pain after cesarean section by TAP Block method

Zanjan University of Medical Sciences0 sites100 target enrollmentStarted: TBDLast updated:

Trial Snapshot

Phase
Phase 3
Status
Recruiting
Enrollment
100

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Ages
18 years to no limit (—)
Sex
All

Inclusion Criteria

  • ASA(American Society of Anesthesiologists) grade 1 or 2
  • The patient's ability to report the extent of their pain by criteria VAS(visual analog scale)
  • Conscious consent of the patient to participate in the study
  • Candidate for cesarean section under anesthesia with TAP(transverse abdominis plane) block

Exclusion Criteria

  • History of anaphylaxis to dexmedetomidine or ropivacaine
  • History of drug abuse
  • History of coagulopathy

Investigators

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