IRCT2015102824754N1CompletedPhase 3
Clinical trial of the effects of misoprostol injection compared with oxytocin injection in the umbilical vein in treatment of placenta retaining after delivery
Conditions
Trial Snapshot
- Phase
- Phase 3
- Status
- Completed
- Enrollment
- 44
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
- Ages
- 18 years to 50 years (—)
- Sex
- Female
Inclusion Criteria
- •During the first and second stages of labor with success, leaving the pair within half an hour after leaving the fetus from the uterus, to obtain written consent from patients to participate in the study
- •Exclusion criteria:
- •Maternal and fetal problems that lead to vaginal delivery is possible. ; Placenta within half an hour after leaving the fetus from the uterus, patient request for exclusion
Exclusion Criteria
- Not provided
Investigators
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