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Clinical Trials/IRCT2015050919037N9
IRCT2015050919037N9
Completed
Phase 2

Comparison of the effect of using and not using of melatonin on prevention of patients' postpartum uterus bleeding after normal vaginal delivery

Investigator0 sites140 target enrollmentTBD
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ConditionsPostpartum haemorrhage.haemorrhage after delivery of fetus or infant

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Postpartum haemorrhage.
Sponsor
Investigator
Enrollment
140
Status
Completed
Last Updated
8 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

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
Investigator

Eligibility Criteria

Inclusion Criteria

  • •Term pregnant women with simultaneous labor pain and hemoglobin level above 10 mg/dl.
  • •Exclusion criteria:
  • •History of underline disease, dystocia, multiparity, chorioamnionitis and need for delivery induction, cesarean section or blood transfusion.

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Not specified

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