Investigation and comparison of neonatal complications of two methods of umbilical cord milking and early cord clamping in neonates
Phase 3
Recruiting
- Conditions
- preterm infants.Preterm [premature] newborn [other]
- Registration Number
- IRCT20180201038586N1
- Lead Sponsor
- Mashhad University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 160
Inclusion Criteria
The infant's parents should give written informed consent for the infant to enter the study
?All infants who are not suspected of placental abruption
For a gestational age of 28 to 34 weeks, in sonography, there should be no sign of placenta previa, anemia, hydrops and embryonic major abnormalities.
Exclusion Criteria
Less than 25 cm length of umbilical cord
Thick meconium
The true knot of the umbilical cord
Major anomalies of umbilical cord
In a case that the infant is not hospitalized in NICU or during the study, the parents do not agree with the presence of their infant in the study
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The amount of transfused blood. Timepoint: The amount of transfused blood in the first 120 hours. Method of measurement: Blood sampling.;The amount of bilirubin. Timepoint: The amount of bilirubin is measured daily. Method of measurement: Blood sampling.
- Secondary Outcome Measures
Name Time Method