Overview
Sublingual Misoprostol to Reduce Blood Loss During Elective Cesarean Delivery
Status:
Unknown status
Unknown status
Trial end date:
2017-05-01
2017-05-01
Target enrollment:
0
0
Participant gender:
Female
Female
Summary
Sublingual Misoprostol to Reduce Blood Loss During Elective Cesarean Delivery : A Randomized Controlled TrialPhase:
Phase 2Accepts Healthy Volunteers?
Accepts Healthy VolunteersDetails
Lead Sponsor:
Ain Shams Maternity HospitalTreatments:
Misoprostol
Ranitidine
Ranitidine bismuth citrate
Criteria
Inclusion Criteria:- singleton pregnancies
- women booked for elective C.S
- full term pregnancies
- primi gravida or previous one delivery ( either by spontaneous vaginal delivery or C.S
)
Exclusion Criteria:
- blood disorders
- multiple pregnancy
- placenta previa
- polyhydramnios
- marked maternal anemia
- contraindications to prostaglandin e.g history of asthma , allergy to misoprostol
- previous 2 or more C.S