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Evaluation of the efficacy and safety of prone ventilation in ARDS patients with three-person

Evaluation of the effectiveness and safety of prone ventilation in patients with ARDS by three-person

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300070205
Enrollment
Unknown
Registered
2023-04-04
Start date
2023-03-23
Completion date
Unknown
Last updated
2023-06-04

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

Conditions

acute respiratory distress syndrome

Interventions

Sponsors

Qilu Hospital of Shandong University Dezhou Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1. Patients with moderate to severe ARDS who meet the 2012 Berlin diagnostic criteria; 2. Patients diagnosed with prone ventilation; 3. Mechanical ventilation >= 24h; 4. Patients or family members were informed and agreed to participate in this study.

Exclusion criteria

Exclusion criteria: 1. Coma, increased intracranial pressure, subarachnoid hemorrhage, arrhythmia, irreversible organ function injury; 2. Asthma, the presence of severe life-threatening hypoxemia, severe obesity, acute bleeding, spinal injury, sternal and pelvic fractures; 3. Recent abdominal surgery; Combined with hemodynamic instability; 4. Other patients who cannot tolerate face-down posture.

Design outcomes

Primary

MeasureTime frame
oxygenation index;

Secondary

MeasureTime frame
heart rate;Edema of the face;Occurrence of stress injury;Catheter anomaly;

Countries

China

Contacts

Public ContactZhang Binbin

Qilu Hospital of Shandong University Dezhou Hospital

zhangbinbinql@163.com+86 185 6008 5288

Outcome results

None listed

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