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Clinical Trials/IRCT201205099697N1
IRCT201205099697N1CompletedPhase 3

The effects of diclofenac suppository and intravenous acetaminophen, and the combination of them, on postoperative pain in patients undergoing spinal anesthesia for cesarean section

Golestan University of Medical Sciences0 sites90 target enrollmentStarted: TBDLast updated:
Conditions

Trial Snapshot

Phase
Phase 3
Status
Completed
Sponsor
Enrollment
90

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Ages
17 years to 40 years (—)
Sex
Female

Inclusion Criteria

  • Patients with 1 and 2 ASA class of Anesthesia; Term gestational age; absence of chronic diseases such as cardiovascular; hepatic and renal disease. exclusion criteria: hypersensitivity to any drug such as acetaminophen; local anesthetics, having liver or renal disease; diabetes, and patients who used analgesic drugs (opioids, NSAID and corticosteroid)within 8 to 12 hours before the intervention

Exclusion Criteria

  • Not provided

Investigators

Sponsor
Golestan University of Medical Sciences

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