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Evaluation of placental transfusion in preterm infants under different delivery modes

Evaluation of placental transfusion in preterm infants under different delivery modes

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000031307
Enrollment
Unknown
Registered
2020-03-27
Start date
2020-09-01
Completion date
Unknown
Last updated
2020-03-30

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

Conditions

Preterm infant

Interventions

experimental group:DCC combined with CPAP
control group:EPT combined with CPAP

Sponsors

Chongqing Health Center for Women and Children
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Very preterm infants (gestational age < 32 weeks) delivered in our hospital.

Exclusion criteria

Exclusion criteria: 1. The parents refuse to sign the informed consent form; 2. Factors of pregnant women: the mother's massive hemorrhage needs emergency rescue, the placenta or umbilical cord has serious abnormality; 3. The fetus's factors: Severe deformity neonate affecting the effect of resuscitation; Newborn requiring immediate tracheal intubation and further resuscitation should be evaluated at birth; 4. All other situations that may affect the safety of mothers and infants will be judged by the obstetrician and pediatrician on site whether they are included in this study.

Design outcomes

Primary

MeasureTime frame
hemoglobin;Placenta rest blood volume;

Secondary

MeasureTime frame
time of HR>100bpm;breath time;Incidence of complications;mortality;

Countries

China

Contacts

Public ContactZhong Xiaoyun

Chongqing Health Center for Women and Children

13883519380@163.com+86 13883519380

Outcome results

None listed

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