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Success factors for improving prognosis by awake prone position in patients infected by Omicron variant

Success factors for improving prognosis by awake prone position in patients infected by Omicron variant

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400089613
Enrollment
Unknown
Registered
2024-09-11
Start date
2023-01-01
Completion date
Unknown
Last updated
2024-09-16

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

Conditions

COVID-19

Interventions

Treatment group:with clinical conduct of APP
Control group:without clinical conduct of APP

Sponsors

The First Affiliated Hospital of Anhui Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years

Inclusion criteria

Inclusion criteria: Patients were included if they were =18 years old, had a laboratory-confirmed diagnosis of COVID-19 by polymerase chain reaction testing, presented oxygen saturation of <93%.

Exclusion criteria

Exclusion criteria: The research phase: Patients discharged or intubated within 24 hours were excluded. The validation phase: We excluded patients who discharged or intubated within 24 hours, were unable or refused to provide informed consent, were haemodynamically unstable, were severely obese with a body-mass index higher than 40 kg/m^2, were pregnant, or had a contraindication to awake prone positioning (recent abdominal or thoracic surgery/trauma, facial/pelvic/spine fractures, untreated pneumothorax, etc).

Design outcomes

Primary

MeasureTime frame
ROX index;

Secondary

MeasureTime frame
mortality rate;

Countries

China

Contacts

Public ContactZhenxing Ding

The First Affiliated Hospital of Anhui Medical University

dingdoctorzx@163.com+86 139 0969 4760

Outcome results

None listed

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