Comparison effect of Carbetocine and Syntometrin in prevention of post partum hemorrhage
Not Applicable
Completed
- Conditions
- Post partum hemorrhage.Postpartum care and examination
- Registration Number
- IRCT138810212854N2
- Lead Sponsor
- Vice Chancellor for research
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 200
Inclusion Criteria
pregnant women with single pregnancy and candidate for vaginal delivery Exclusion criteria: Presence of preeclampsia, hypotension, heart disease, asthma, hypertonic uterus, uterine rupture, or vaginal and cervical laceration, being high risk for postpartum bleeding such as: multiparity, uterine myoma, history of postpartum bleeding, or need for uterine curettage.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method terine tone. Timepoint: 0.5 and 1 hours after delivery. Method of measurement: Assessment of uterine tone.;Hemoglobin level. Timepoint: Before and 24 hours after delivery. Method of measurement: Hemoglobine assessment.
- Secondary Outcome Measures
Name Time Method eed to adminestration of utertonic drug. Timepoint: During 24 hours after delivery. Method of measurement: dosage and amount of drug.;Adverse effects. Timepoint: During Hospitalization. Method of measurement: Observation of adverse effects.