Skip to content

Efficacy and safety of modified Lisa in the treatment of RDS

Efficacy and safety of modified Lisa in the treatment of RDS

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100047885
Enrollment
Unknown
Registered
2021-06-27
Start date
2021-07-01
Completion date
Unknown
Last updated
2022-03-07

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

Conditions

respiratory distress syndrome

Interventions

Modified LISA group:Extended administration
Control group:No

Sponsors

Shenzhen Second People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Gestational age<=34 weeks; 2. Meet the RDS diagnostic criteria of "Practical Neonatology" (5th Edition): (1) Progressive dyspnea in premature infants after birth; (2) Consistent with RDS chest X-ray findings.

Exclusion criteria

Exclusion criteria: 1. Children who need endotracheal intubation or have been intubated; 2. Children with respiratory distress caused by severe infection, aspiration pneumonia asphyxia, congenital pneumonia, etc.; 3. Combined with severe congenital malformations (such as congenital pulmonary dysplasia, respiratory malformation, esophageal fistula, etc.); 4. Serious complications such as early-onset sepsis, severe intracranial hemorrhage; 5. Congenital hereditary shooting disease; 6. Endotracheal intubation and mechanical ventilation are required during postnatal resuscitation and exogenous PS has been used before admission.

Design outcomes

Primary

MeasureTime frame
Intubation rate;Necrotizing enterocolitis;

Secondary

MeasureTime frame
Non-invasive ventilation time;Oxygen therapy time;Decreased oxygen saturation;bradycardia;air leak syndrome;bronchopulmonary dysplasia;Retinopathy;

Countries

China

Contacts

Public ContactLiu Rongtian

Shenzhen Second People's Hospital

cytt1982@163.com+86 15018503430

Outcome results

None listed

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