Bilateral uterine compression to reduce blood loss and prevent postpartum haemorrhage after vaginal delivery
Phase 3
Recruiting
- Conditions
- prevention of postpartum hemorrhagebilateral uterine compression,postpartum hemorrage ,uterotonics
- Registration Number
- TCTR20140515002
- Lead Sponsor
- khalid abd aziz mohamed
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 320
Inclusion Criteria
Gestational age more than 28 weeks the gestational age was determined based upon the date of the first day of last normal menstrual period and confirmed by ultrasound scan during the 1st trimester
Women at high risk for primary atonic postpartum hemorrhage
Over distended uterus
Large fetus
Multiple fetuses
Hydraminos
Distension with clots accidental hemorrhage
Exhausted myometrium
Prolonged labor
Oxytocin or prostaglandin stimulation
Chorioamnionitis
Previous uterine atony
Placenta previa
Marked anemia
Exclusion Criteria
Postpartum hemorrhage
Retained placenta
Coagulopathy
Chronic medical illness hepatic renal
Pregnancy induced hypertension PIH
Refusal to participate in the study
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Blood loss > 500 ml after enrolment. Mean blood loss after enrolment (up to 30 and 60 minutes). at time of delivery using a questionnaire interview
- Secondary Outcome Measures
Name Time Method number of patients needig additional uterotonics and blood trasfusion at time of delivery using a questionnaire interview