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Cord Milking in Elective Cesarean Section

Conditions
Placental Transfusion
Interventions
Procedure: Umbilical cord milking
Registration Number
NCT03668782
Lead Sponsor
Policlinico Abano Terme
Brief Summary

The objective of the study was to investigate the efficacy and safety of umbilical cord milking as compared with immediate cord clamping on placental transfusion, estimated by Δ hematocrit between cord blood at birth and capillary heel hematocrit at 48 hours of age, in elective cesarean delivered neonates.

Detailed Description

Not available

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
130
Inclusion Criteria

singleton low risk pregnancy, gestational age of 39 to 40/0 weeks confirmed by a first trimester ultrasound, no evidence of active labor, 18 years of age, and (5) a written consent given by the woman.

Exclusion Criteria

maternal medical and obstetric complications, severe anemia, clotting disorders and suspected intrauterine growth restriction

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
umbilical cord milking.Umbilical cord milkingTthe umbilical cord of neonates was milked.
immediate cord clampingUmbilical cord milkingTthe umbilical cord of neonates was cut and clamped.
Primary Outcome Measures
NameTimeMethod
Placental transfusion48 hours

Δ hematocrit between cord blood at birth and capillary heel hematocrit at 48 hours of age

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Policlinico Abano Terme

🇮🇹

Abano Terme, Italy

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