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Clinical Trials/IRCT201211187013N2
IRCT201211187013N2Completed未知

?Effect of Preventive Analgesia with Paracetamol in Post-Cesarean Section Pain Control

Women's Reproductive Research Center, Tabriz University of Medical Sciences0 sites100 target enrollmentStarted: TBDLast updated:
Conditions

Trial Snapshot

Phase
未知
Status
Completed
Sponsor
Enrollment
100

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Ages
18 years to 40 years (—)
Sex
Female

Inclusion Criteria

  • Term parturients; Parturients with over 18 years; Parturients undergoing elective cesarean section with spinal anesthesia.
  • Exclution criteria:
  • To have a contraindication for spinal anesthesia; To have allergy to local anesthetics; Patients with mental disorders; Patients with organic dysfunctions; Previous chronic pain; Rased hepatic enzyms.

Exclusion Criteria

  • Not provided

Investigators

Sponsor
Women's Reproductive Research Center, Tabriz University of Medical Sciences

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