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Efficacy and safety of early prone positioning combined with HFNC or NIV in moderate to severe ARDS: a pilot Multi-center prospective cohort study

Efficacy and safety of early prone positioning combined with HFNC or NIV in moderate to severe ARDS: a pilot Multi-center prospective cohort study

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900023564
Enrollment
Unknown
Registered
2019-06-02
Start date
2019-09-01
Completion date
Unknown
Last updated
2019-06-03

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

Conditions

ARDS

Interventions

2:NIV

Sponsors

Beijing Chao-Yang Hospital affiliated to Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: The diagnosis of ARDS was made when a patient met the Berlin definition criteria: (1) presence of acute hypoxemic respiratory failure; (2) onset within 7days of insult, or new (within 7days) or worsening respiratory symptoms; (3) bilateral opacities on chest x-ray or CT not fully explained by effusions, lobar or lung collapse, or nodules; and (4) cardiac failure not the primary cause of acute respiratory failure.patients were included when their PFR were less than 200mmHg.

Exclusion criteria

Exclusion criteria: (1) The patients who do not agree to participate in the research. (2) The patients who can not cooperate with treatment.

Design outcomes

Primary

MeasureTime frame
PaO2/FiO2;

Countries

China

Contacts

Public ContactHe Hang-Yong

Beijing Institute of Respiratory Medicine, Beijing Chao-Yang Hospital

yonghang2004@sina.com+86 13693585722

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 28, 2026