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Cord Milking in Elective Cesarean Section

P

Policlinico Abano Terme

Status

Unknown

Conditions

Placental Transfusion

Treatments

Procedure: Umbilical cord milking

Study type

Observational

Funder types

Other

Identifiers

NCT03668782
24/2018 Fondazione Leonardo

Details and patient eligibility

About

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.

Enrollment

130 estimated patients

Sex

All

Ages

1 minute to 2 days old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

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

Trial design

130 participants in 2 patient groups

immediate cord clamping
Description:
Tthe umbilical cord of neonates was cut and clamped.
Treatment:
Procedure: Umbilical cord milking
umbilical cord milking.
Description:
Tthe umbilical cord of neonates was milked.
Treatment:
Procedure: Umbilical cord milking

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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