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The clinical study of sustain lung inflation in neonatal respiratory distress syndrome in premature neonates

The clinical study of sustain lung inflation in neonatal respiratory distress syndrome in premature neonates

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1800020125
Enrollment
Unknown
Registered
2018-12-15
Start date
2017-08-01
Completion date
Unknown
Last updated
2018-12-18

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

Conditions

Neonatal respiratory distress syndrome

Interventions

experimental group:IN-SUR-E+SLI
Control group:IN-SUR-E alone

Sponsors

Women and Children Health Care Hospital of Dongguan
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. gestational age from 24 weeks to 32 weeks and birth weight =1500g; 2. diagnosis of respiratory distress syndrome by clinical syndrome and X-ray; 3. the agreement and signature of parents; 4. failure by continuous positive airway pressure(CPAP) within 24 hours.

Exclusion criteria

Exclusion criteria: 1. neonates who accepted endotracheal intubation in the delivery room; 2. severe congenital malformation such as severe heart failure and so on.

Design outcomes

Primary

MeasureTime frame
the mechanical ventilation re-intubation rate within 72 hours after extubation;—

Secondary

MeasureTime frame
mechanical ventilation time;noninvasive ventilation time;hospital stays;complications of premature;blood gas;—

Countries

China

Contacts

Public ContactLi Minxu

Dongguan Women and Children Health Care Hospital

dgminxu@163.COM+86 13316680511

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 19, 2026