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A randomized controlled study of noninvasive ventilator in the treatment of neonatal respiratory failure at high altitude

A randomized controlled study of noninvasive ventilator in the treatment of neonatal respiratory failure at high altitude

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400082086
Enrollment
Unknown
Registered
2024-03-20
Start date
2022-05-11
Completion date
Unknown
Last updated
2024-03-25

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

Conditions

Neonatal respiratory failure

Interventions

Nasal Continuous Positive Airway Pressure Group:Nasal Continuous Positive Airway Pressure
Nasal Intermittent Positive Pressure Ventilation Group:Nasal Intermittent Positive Pressure Ventilation

Sponsors

Changdu People's Hospital of Tibet
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Gestational age 24 weeks to 42 weeks, after birth to 28 days 2. Non-invasive NIPPV and NCPAP ventilation after birth 3. Postnatal patients received any mode of invasive mechanical ventilation through tracheal intubation, and the first extubation was performed to disengage from invasive ventilation 4. Parents sign informed consent.

Exclusion criteria

Exclusion criteria: 1. Congenital malformations that affect the work of breathing 2. Neuromuscular disorders that affect the work of breathing 3.The structure of upper respiratory tract was abnormal 4. Intubation is needed after extubation due to surgical procedures 5. Presence of active intraventricular hemorrhage

Design outcomes

Primary

MeasureTime frame
Intubation rate needed within 48 hours of NIPPV and CPAP;Rate of reintubation within 48 hours after extubation;Rate of BPD;mortality;Incidence of patent ductus arteriosus;

Secondary

MeasureTime frame
Air leakage rate;Necrotizing enterocplitis;

Countries

China

Contacts

Public ContactWang Yong Ming

Changdu People's Hospital of Tibet

379020633@qq.com+86 138 8392 5221

Outcome results

None listed

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