The effect of umbilical cord milking on neonatal outcome in preterm infants

Not Applicable

Completed

Conditions: P07.30
Preterm infant.
Preterm newborn, unspecified weeks of gestation

Registration Number: IRCT2017072031697N1

Lead Sponsor: Hoemozgan University of Medical Sciences

Brief Summary: Not available

Detailed Description: Not available

Recruitment & Eligibility

Status: Complete

Sex: Female

Target Recruitment: 80

Inclusion Criteria

All pregnant women 28 to 34 weeks of gestation (based on the first trimester ultrasonography of pregnancy). Exclusion criteria: Short cord (less than 25 cm); Vigorous or meconium stained; congenital major anomalies; Umbilical cord prolapse; Phytoplasmic hydrops; multiple pulmonary deliveries; maternal ABO or negative Rh mother; mothers with placenta and decollete pair; mothers Abnormal umbilical cord such as a true knot; mothers with underlying illnesses; Such as diabetes and high blood pressure; Not being a resident of Hormozgan or lack of follow-up.

Exclusion Criteria

Not provided

Study & Design

Study Type: interventional

Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Hemoglobin premature infants. Timepoint: 48 hours after birth. Method of measurement: According to the results reported by the laboratory of Shariati Hospital and expressed in grams per liter of blood.

Secondary Outcome Measures

Name	Time	Method
Intrauterine pulmonary edema. Timepoint: After birth. Method of measurement: Intravenous hemorrhage of the baby, expressed on the basis of sonography.;Infant hematocrit. Timepoint: 48 hours after birth. Method of measurement: Based on the results reported by Shariati Hospital's laboratory, it is expressed in terms of percentage and number.;Primary neonatal hypertension. Timepoint: After birth. Method of measurement: Based on the report reported by Shariati Hospital's laboratory based on mmHg and with the number.