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Prostaglandin
15-methyl prostaglandin F2α for Postpartum Hemorrhage
Phase 4
Waitlist Available
Led By Naida M Cole, MD
Research Sponsored by Brigham and Women's Hospital
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up within the first 24 hours after delivery of the fetus
Awards & highlights
Study Summary
This study is evaluating whether a medication may help reduce bleeding after childbirth.
Eligible Conditions
- Postpartum Hemorrhage
- Uterine Atony
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ at 5 minutes following administration of the first study drug
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~at 5 minutes following administration of the first study drug
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Secondary outcome measures
Additional Intervention
Additional Uterotonic
Hematocrit Drop
+5 moreTrial Design
2Treatment groups
Active Control
Group I: 15-methyl prostaglandin F2αActive Control2 Interventions
IM Carboprost followed by Methylergonovine if needed.
Group II: Methylergonovine MaleateActive Control2 Interventions
IM Methylergonovine followed by Carboprost if needed.
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Who is running the clinical trial?
Brigham and Women's HospitalLead Sponsor
1,614 Previous Clinical Trials
11,470,735 Total Patients Enrolled
4 Trials studying Postpartum Hemorrhage
167 Patients Enrolled for Postpartum Hemorrhage
Naida M Cole, MDPrincipal InvestigatorBrigham and Women's Hospital, 75 Francis Street, Boston MA 02115
1 Previous Clinical Trials
100 Total Patients Enrolled
1 Trials studying Postpartum Hemorrhage
100 Patients Enrolled for Postpartum Hemorrhage
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