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High frequency oscillatory ventilation versus traditional mechanical ventilation in premature infant with respiratory distress syndrome based on volume assurance: a randomized crossover clinical trial

High frequency oscillatory ventilation versus traditional mechanical ventilation in premature infant with respiratory distress syndrome based on volume assurance: a randomized crossover clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200059430
Enrollment
Unknown
Registered
2022-04-29
Start date
2022-05-01
Completion date
Unknown
Last updated
2024-03-04

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

Group A:Traditional mechanical ventilation (A/C-VG) mode was used for 2 hours, followed by high-frequency oscillation ventilation (HFOV-VG) mode for 2 hours
Group B:High-frequency oscillation ventilation (HFOV-VG) mode was used for 2 hours, followed by traditional mechanical ventilation (A/C-VG) mode for 2 hours

Sponsors

Children's Hospital of Chongqing Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Premature infants who are diagnosed with respiratory distress syndrome within 12 hours after birth and need tracheal intubation for mechanical ventilation; 2. Gestational age 23-32 weeks; 3. Parents sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. There are congenital malformations that affect respiratory function, such as congenital heart disease; 2. Inherited metabolic diseases; 3. There are structural abnormalities of the upper respiratory tract; 4. Intubation is required due to surgery; 5. Severe suffocation; 6. Moderate or above HIE.

Design outcomes

Primary

MeasureTime frame
percutaneous carbon dioxide partial pressure;

Countries

China

Contacts

Public ContactShi Yuan

Children's Hospital of Chongqing Medical University

petshi530@vip.163.com+86 23 63635177

Outcome results

None listed

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