Clinical study of prone ventilation in critically ill COVID-19 patients undergoing mechanical ventilation

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR2200059735

Enrollment

Unknown

Registered

2022-05-10

Start date

2022-04-30

Completion date

Unknown

Last updated

2024-03-25

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

Conditions

Critical type COVID - 19

Interventions

None listed

Eligibility

Sex/Gender

All

Age

18 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1. Meet the diagnostic criteria of "severe pneumonia"; 2. The age ranged from 18 to 85 years; 3. No gender limitation; 4. Patients receiving mechanical ventilation; 5. Long range prone ventilation treatment ( > 24h).

Exclusion criteria

Exclusion criteria: 1. Prone ventilation contraindications, such as severe intra-abdominal hypertension, multiple trauma with unstable fractures, severe hemodynamic instability and confirmed venous thromboembolism, and anticoagulant treatment for less than 2 days; 2. Pregnancy status; 3. Patients considered unsuitable for the study by the researcher.

Design outcomes

Primary

Measure	Time frame
Oxygenation index;	—

Secondary

Measure	Time frame
Respiratory static compliance;Airway resistance;Thoracic effusion;Enteral nutrition tolerance;Cardiac parameters;Inflammatory factor levels;	—

Countries

China

Contacts

Public ContactYingchuan Li

Shanghai Tenth People's Hospital

yingchuan.li@sjtu.edu.cn+86 13681945425

Outcome results