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Clinical Trials/IRCT138812043413N1
IRCT138812043413N1
Completed
未知

Comparison two methods of oxytocin use after delivery

Kashan University of Medical Sciences, Vice-chancellor for Research0 sites200 target enrollmentTBD

Overview

Phase
未知
Intervention
Not specified
Conditions
control of third stage.
Sponsor
Kashan University of Medical Sciences, Vice-chancellor for Research
Enrollment
200
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
Kashan University of Medical Sciences, Vice-chancellor for Research

Eligibility Criteria

Inclusion Criteria

  • woman with vaginal delivery after 20 week gestation without instrumentation, age between 18 and 40 yrs, singleton pregnancies, parity equal or less than 5, Iranian nationality.
  • Exclusion criteria: Allergy to oxytocin, Presence of any medical or obstetric diseases (including pregnancy\-induced hypertension disorders, hypertention, heart diseases, coagulation disorder), known risk factors for postpartum haemorrhage (including abnormal placentation, uterine fibroids, history of postpartum hemorrhage or uterine atony, polyhydramnious , clinical chorioamnionitis , precipitant labor)

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Not specified

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