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Clinical Trials/IRCT20231228060548N1
IRCT20231228060548N1CompletedPhase 3

Investigating the effect of adding metoclopramide to subcutaneous lidocaine on pain after lower abdominal surgery with general anesthesia

Islamic Azad University0 sites58 target enrollmentStarted: TBDLast updated:
Conditions

Trial Snapshot

Phase
Phase 3
Status
Completed
Enrollment
58

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Ages
15 years to 75 years (—)
Sex
All

Inclusion Criteria

  • Being 15-75 years old
  • Signing a written informed consent form to enter the study
  • 1 and 2 ASA
  • Non-use of drugs and alcohol
  • Elective surgery

Exclusion Criteria

  • Decreased level of consciousness
  • Hemodynamic disorder
  • Abnormal intraoperative bleeding
  • Length of operation more than 4 hours

Investigators

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