Comparison of the effects of intramuscular methylergonovine, intravascular oxytocin, and sublingual prostaglandin in prevention of post partum hemorrhage
Phase 2
- Conditions
- Post partum haemorrhage.Other immediate postpartum haemorrhage
- Registration Number
- IRCT201106143756N2
- Lead Sponsor
- Jundishapour University Of Medical Scienses
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 150
Inclusion Criteria
women with singleton pregnancy; low risk pregnancies;live fetuses; cephalic presentation; normal blood pressure;no history of postpartum haemorrhage;no history of coagulation disorders;no history of heart disease;no history of seizure; no sever anemia(Hb less than 7)
exclusion criteria:
uterine atonia ;large lacerations with massive bleeding
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Volume of Postpartum haemorrhage. Timepoint: One hour after delivery. Method of measurement: Scaled container and scaling of the pad in mililiter.;Amount of hemoglobin drop. Timepoint: 24 houres after delivery. Method of measurement: Check of hemoglobin.;Duration of the third phase of parturation. Timepoint: From fetus delivery to expression of placenta. Method of measurement: Check of the time in second.
- Secondary Outcome Measures
Name Time Method ausia , vomitting, diarrhia and fever due to misoprostole. Timepoint: 1 and 2 hour after delivery. Method of measurement: Patient's symptoms and vital siqns.;Hypotension and water intoxication. Timepoint: 1 and 2 hour after delivery. Method of measurement: Patient's symptoms and vital siqns.;Transient hypertension due to metergin. Timepoint: 1 and 2 hour after delivery. Method of measurement: Patient's symptoms and vital siqns.