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Application and Optimization of a Pressure Injury Prevention Protocol for ARDS Patients Undergoing Prone Ventilation

Application and Optimization of a Pressure Injury Prevention Protocol for ARDS Patients Undergoing Prone Ventilation

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500101498
Enrollment
Unknown
Registered
2025-04-25
Start date
2024-08-05
Completion date
Unknown
Last updated
2025-04-28

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

Conditions

Pressure injury

Interventions

intervention group:A pressure injury prevention plan
control group:Routine preventive measures

Sponsors

Zhongshan Hospital Affiliated to Fudan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. ARDS patients who meet the Berlin diagnostic criteria; 2. Age >= 18 years old; 3. Patients who plan to undergo prone position ventilation and have been receiving treatment for prone position ventilation for >= 1 day; 4. There is no pressure damage to the skin during prone position ventilation; 5. Patients or their family members sign informed consent forms related to this trial.

Exclusion criteria

Exclusion criteria: Pregnant or lactating women

Design outcomes

Primary

MeasureTime frame
The incidence of pressure injury;

Secondary

MeasureTime frame
Knowledge and attitude level of stress injury prevention among ICU nurses;

Countries

China

Contacts

Public ContactWei Qin

Zhongshan Hospital, Fudan University

qin.wei@zs-hospital.sh.cn+86 136 6165 2348

Outcome results

None listed

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