MedPath

misoprostol efficiency in postpartum hemorrhage.

Phase 4
Conditions
postpartum hemorrhage
Registration Number
PACTR201812901591120
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
400
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

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
© Copyright 2025. All Rights Reserved by MedPath