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A clinical study on prediction prone positioning response in acute respiratory distress syndrome patients

A clinical study on prediction prone positioning response in acute respiratory distress syndrome patients

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-ROC-16009073
Enrollment
Unknown
Registered
2016-08-24
Start date
2016-08-15
Completion date
Unknown
Last updated
2017-04-18

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

Case series:Prone positioning ventilation

Sponsors

West China Hospital of Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. aged 18 years or more; 2. diagnosis of severe ARDS: (1) Within 1 week of a known clinical insult or new or worsening respiratory symptoms; (2) Bilateral opacitiesnot fully explained by effusions, lobar/lung collapse, or nodules; (3) Respiratory failure not fully explained by cardiac failure or fluid overload Need objective assessment (eg, echocardiography) to exclude hydrostatic edema if no risk factor present; (4) PaO2/FiO2=150mmHg,PPEP=5cmH2O.

Exclusion criteria

Exclusion criteria: 1. Hemodynamic instability: Cardiac pacemaker inserted in the last 2 days or life-threatening arrhythmias or circulatory disorders (use of large doses of vasoactive drugs); 2. Intracranial pressure >30 mm Hg or cerebral perfusion pressure <60 mmHg; 3. Massive hemoptysis requiring an immediate surgical or interventional radiology procedure; 4. Tracheal surgery or sternotomy during the previous 15 days; 5. Serious facial trauma or facial surgery; 6. Deep venous thrombosis treated for less than 2 days; 7. Anterior chest wall placed closed thoracic drainage device; 8. Open wound of abdominal cavity; 9. Unstable spine; 10. femur or pelvic fractures; 11. Pregnant women; 12. Use of extracorporeal membrane oxygenation (ECMO) before inclusion; 13. Chronic respiratory failure requiring oxygen therapy or non-invasive ventilation(NIV); 14. Previous inclusion in the present study; 15. Opposition from next of kin.

Design outcomes

Primary

MeasureTime frame
PaO2;PaCO2;

Countries

China

Contacts

Public ContactTingting Liu

West China Hospital, Sichuan University

liutingting_rt@126.com+86 13982230775

Outcome results

None listed

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