Skip to content

A single-center prospective study of heated humidified high-flow nasal cannula and nasal continuous positive airway pressure for RDS

A single-center prospective study of heated humidified high-flow nasal cannula and nasal continuous positive airway pressure for RDS

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200066494
Enrollment
Unknown
Registered
2022-12-07
Start date
2022-12-07
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

respiratory distress syndrome

Interventions

HHHFNC group:The initial respiratory support was HHHFNC mode
NCPAP group:The initial respiratory support was CPAP mode

Sponsors

Shenzhen Second People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 1 Years

Inclusion criteria

Inclusion criteria: A. Gestational age 28-36+6 weeks. B. Meet the RDS diagnostic criteria of Practical Neonatology (5th edition) : a. Progressive dyspnea of premature infants after birth; b. Chest X-ray findings consistent with RDS: C. within 6 h after birth into the line of endotracheal intubation and noninvasive respiratory support, inhaled oxygen concentration (fraction of inspired oxygen, FiO2) ? 30%.

Exclusion criteria

Exclusion criteria: A. Children who require or have been intubated immediately after birth; B. Children with respiratory distress due to severe infection, aspiration pneumonia asphyxia, congenital pneumonia and other causes; C. Complicated with severe congenital malformations (such as cyanosis congenital heart disease, congenital pulmonary dysplasia, respiratory malformations, esophageal fistula, etc.); D. Meconium inhalation syndrome, early-onset sepsis, severe intracranial blood; E. congenital hereditary ejection; F. Endotracheal intubation mechanical ventilation was required at postnatal resuscitation and exogenous PS was used before admission; G.Neonatal pulmonary hemorrhage, cardiac arrest, cardiopulmonary resuscitation, still does not establish effective spontaneous breathing in children.

Design outcomes

Primary

MeasureTime frame
Reintubation rate within 72 hours;

Secondary

MeasureTime frame
Blood Gas Analysis;Utilization rate of Poractant Alfa Injection;Incidence of complications;Time of oxygen therapy;mortality rate;the score of NBNA;Skull color ultrasound or magnetic resonance imaging;Bailey Infant Neurodevelopmental Score;Indicators of moisture respiratory lung function;The incidence of asthmatic disease;

Countries

China

Contacts

Public ContactBai Yuxin

Shenzhen Second People's Hospital

Baiyuxin0417@163.com+86 13823235533

Outcome results

None listed

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