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Clinical Trials/IRCT20120215009014N455
IRCT20120215009014N455
Recruiting
Phase 3

Comparison of the effect pethidine, paracetamol and their combination on the reduction of labor pain and the level of satisfaction of primiparous women

Hamedan University of Medical Sciences0 sites111 target enrollmentTBD

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Not specified
Sponsor
Hamedan University of Medical Sciences
Enrollment
111
Status
Recruiting
Last Updated
3 years ago

Overview

Brief Summary

No summary available.

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

Investigators

Eligibility Criteria

Inclusion Criteria

  • Age of 18 to 40 years
  • Term pregnancy
  • A singleton with a cephalic display
  • Cervical dilatation 4 cm
  • Pregnant women undergoing induction of labor with oxytocin

Exclusion Criteria

  • Analgesic consumption in the last 24 hours
  • Preeclampsia and eclampsia
  • Severe obesity
  • Intrauterine fetal death
  • Fetal abnormalities

Outcomes

Primary Outcomes

Not specified

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