Overview

Sublingual Misoprostol to Reduce Blood Loss During Elective Cesarean Delivery

Status:
Unknown status
Trial end date:
2017-05-01
Target enrollment:
0
Participant gender:
Female
Summary
Sublingual Misoprostol to Reduce Blood Loss During Elective Cesarean Delivery : A Randomized Controlled Trial
Phase:
Phase 2
Accepts Healthy Volunteers?
Accepts Healthy Volunteers
Details
Lead Sponsor:
Ain Shams Maternity Hospital
Treatments:
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