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Delayed Cord Clamping in Infants Born by 'Two-step' Vaginal Delivery

P

Policlinico Abano Terme

Status

Completed

Conditions

Hematocrit Anemia
Placental Transfusion

Treatments

Procedure: Cord clamping

Study type

Interventional

Funder types

Other

Identifiers

NCT04351997
3158/AT/14

Details and patient eligibility

About

The investigators conducted a RCT (parallel group study with 1:1 randomisation) comparing ECC (at 60 seconds) and DCC (at 180 seconds) in 90 cases of normal birth by' two-step' delivery. In term infants born by' two-step' delivery, DCC results is a higher blood volume in the newborn and facilitates the maternal-placental-fetal exchange of circulating compounds, without potentially detrimental neonatal outcomes.

Full description

Introduction: Placental transfusion supports an important blood transfer to the neonate, promoting a more stable and smooth transition from fetal to extra-uterine life with the potential to prevent iron deficiency in young children. Several studies have demonstrated that cord clamping timing is greatly relevant for facilitate placental transfusion, the transfer of extra blood from the placenta to the infant in the third stage of labor. Therefore, during natural 'two-step' delivery umbilical cord management may play a relevant role on blood passage to the neonate and it may affect neonatal hematological values and placental transfusion. The most effective way to manage umbilical cord in in 'two-step' delivery remains to be established.

Objective: The aim of the present study is to evaluate the effect of two different methods of umbilical cord management (Early Cord Clamping - ECC vs. Delayed Cord Clamping - DCC) on the placental transfusion, defined by in two-step delivery, by ∆ haematocrit (Hct) from arterial cord blood at birth and capillary blood at 48 h of age. Accounting for physiological body weight decrease. Secondary outcomes included contemporary estimate of blood gases, lactate, and glucose concentrations in arterial cord blood gas analysis.

Material and methods: This is a randomized clinical trial on the effect of different cord management newborns born by 'two-step' delivery. After obtaining parental consent, all mothers > 38 weeks' gestation will be assigned to either ECC or DCC group in a 1:1 ratio according to a randomized sequence generated by an opened, sealed, numbered, opaque envelope containing the cord clamping interventions allocation, ECC (at 1 minute) or DCC (at 3 minutes after delivery).

Enrollment

90 patients

Sex

All

Ages

2 to 2 days old

Volunteers

No Healthy Volunteers

Inclusion criteria

Vaginal delivery Gestational age >37 weeks Natural process of labor

Exclusion criteria

Cesarean section Fetal distress Major isoimmunisation Ccongenital diseases Cord abnormalities.

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

90 participants in 2 patient groups

Early cord clamping
Experimental group
Description:
Cord clamping at 60 seconds after birth.
Treatment:
Procedure: Cord clamping
Delayed cord clamping
Experimental group
Description:
Cord clamping at 180 seconds after birth,
Treatment:
Procedure: Cord clamping

Trial contacts and locations

3

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Data sourced from clinicaltrials.gov

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