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Comparing the efficacy of different surfactant on critical neonatal respiratory distress syndrome

Comparing the efficacy of different surfactant on critical neonatal respiratory distress syndrome

Status
Active, not recruiting
Phases
Phase 4
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OPN-17011344
Enrollment
Unknown
Registered
2017-05-09
Start date
2017-05-22
Completion date
Unknown
Last updated
2017-05-22

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

calsurf group and curosurf group:surfactant therapy

Sponsors

Huazhong University of Science and Technology Affiliate Tongji Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. infants <34 weeks gestation; 2. the diagnosis of neonatal respiratory distress syndrome is confirmed,and III or IV level on chest X-ray.

Exclusion criteria

Exclusion criteria: Exclusion criteria are repeated convulsions, coma or intracranial hemorrhage; or Combined with other severe life-threatening diseases, or severe poisoning symptoms and gastrointestinal bleeding

Design outcomes

Primary

MeasureTime frame
blood gas analysis;BPD;complication;

Countries

China

Contacts

Public ContactChang Liwen

Tongji hospital of Huazhong University of Science and Technology

lwchang@tjh.tjmu.edu.cn+86 13971619293

Outcome results

None listed

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