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Clinical Trials/PACTR201812901591120
PACTR201812901591120
Completed
Phase 4

The comparison of efficiency of misoprostol used in different ways in postpartum hemorrhage.

Not provided0 sites400 target enrollmentNovember 29, 2018
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Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Not specified
Sponsor
Not provided
Enrollment
400
Status
Completed
Last Updated
2 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
November 29, 2018
End Date
TBD
Last Updated
2 years ago
Study Type
Interventional
Sex
Female

Investigators

Sponsor
Not provided

Eligibility Criteria

Inclusion Criteria

  • •1\. Pregnant women between the ages of 18\-40
  • •2\. Having pregnancy between 37\-42 weeks
  • •3\. Women on vaginal delivery
  • •4\. Pregnant women with BMI \<35
  • •5\. Nulliparity

Exclusion Criteria

  • •1\. Women with multiple pregnancy
  • •2\. Pregnant women with myoma
  • •3\. Pregnant women with polyhydramnios
  • •4\. Pregnant women with chorioamnionitis
  • •5\. Pregnant women with placental abnormalities
  • •6\. Pregnant women with bleeding diathesis
  • •7\. Pregnant women with caesarean
  • •8\. Pregnant women with low platelet
  • •9\. Women who do not want to participate
  • •10\. Pregnant women with allergic reactions to drug

Outcomes

Primary Outcomes

Not specified

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