to check effect on blood loss on labor
Phase 3
- Conditions
- Health Condition 1: O80- Encounter for full-term uncomplicated delivery
- Registration Number
- CTRI/2024/08/072039
- Lead Sponsor
- nil
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Inclusion Criteria
The following women undergoing vaginal birth will be eligible for enrollment in the study:
Gestation greater than 35 weeks of gestation
Singleton gestation
Last Hb during pregnancy more than 8.0 gm/dl
Exclusion Criteria
Pregnant women with coagulopathy and bleeding disorder
Pregnant women with APH (Placenta previa, placental abruption, uterine rupture and vasa previa)
Fetal distress
Severe FGR (fetal growth retardation
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Primary outcome <br/ ><br>Maternal mean blood loss during delivery at 0 <br/ ><br>Neonatal outcome <br/ ><br>Birth weight within 5 minutes <br/ ><br>Apgar score within 5 minutes <br/ ><br>Need for phototherapy after delivery <br/ ><br>Neonatal intensive care unit admission <br/ ><br>Packed cell volume in neonate at 6+2 hours of age will be done <br/ ><br>Timepoint: Primary outcome <br/ ><br>Maternal mean blood loss during delivery at 0 <br/ ><br>Neonatal outcome <br/ ><br>Birth weight within 5 minutes <br/ ><br>Apgar score within 5 minutes <br/ ><br>Need for phototherapy after delivery <br/ ><br>Neonatal intensive care unit admission <br/ ><br>Packed cell volume in neonate at 6+2 hours of age will be done <br/ ><br>
- Secondary Outcome Measures
Name Time Method eonatal outcome <br/ ><br>Birth weight <br/ ><br>Apgar score <br/ ><br>Need for phototherapy <br/ ><br>Neonatal intensive care unit admission <br/ ><br>Packed cell volume in neonate at 6+2 hours of age will be done <br/ ><br>Timepoint: at zero hours that is at the time of delivery