Skip to main content
Clinical Trials/IRCT201405262624N17
IRCT201405262624N17
Completed
Phase 3

Clinical trial of comparison between the effect of paracetamol (Apotel) and meperidine ( pethidine) on the pain in the first 24 hours after cesarean section.

Vice chancellor for research ,Iran University of Medical Sciences.0 sites100 target enrollmentTBD

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Cesarean delivery.
Sponsor
Vice chancellor for research ,Iran University of Medical Sciences.
Enrollment
100
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

No summary available.

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

Investigators

Sponsor
Vice chancellor for research ,Iran University of Medical Sciences.

Eligibility Criteria

Inclusion Criteria

  • all patients after cesarean section with normal body mass index( between 18\.5 and 25\).
  • Exclusion criteria: Drug abuse; history of allergy to paracetamol or mepiridine; history of hepatitis; renal failure; heart failure; respiratory disease;CNS disorders; coagulopathy; sedative use; psychiatric disorders and complication of cesarean section.

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Not specified

Similar Trials