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The efficacy and safety of physiologically based cord clamping in infants with congenital diaphragmatic hernia (CDH): a prospective, randomized study

The efficacy and safety of physiologically based cord clamping in infants with congenital diaphragmatic hernia (CDH): a prospective, randomized study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0007179
Enrollment
80
Registered
2022-04-12
Start date
2021-10-18
Completion date
Unknown
Last updated
2022-05-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Procedure/Surgery : ? Control group: Immediate umbilical cord clamping after birth followed by intubation and mechanical ventilation ? Intervention group: Physiologically based cord clamping (Intubate

Sponsors

Asan Medical Center
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: ? Antenatal diagnosis of CDH with care in the Fetal Treatment Center ? Gestational age =35 weeks at birth and birth weight = 2 kg

Exclusion criteria

Exclusion criteria: ? Chromosomal anomalies ? Maternal diagnosis with placenta previa, accreta, or abruption ? Clinicians concern for the clinical care of the mother or infant, or study team not available.

Design outcomes

Primary

MeasureTime frame
Decreased in mortality or ECMO rate

Secondary

MeasureTime frame
arterial blood gas analysis;Oxygenation index;Use of inotropics;Duration of mechanical ventilation;Pulmonary hypertension confirmed by echocardiography;NIRS (rScO2)

Countries

Korea, Republic of

Contacts

Public ContactJiyoon Jeong

Asan Medical Center

jjiyunee@hanmail.net+82-2-3010-4770

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026