Study on the application of new assistive devices in prone maneuver of patients with acute respiratory distress syndrome

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR2100045825

Enrollment

Unknown

Registered

2021-04-25

Start date

2021-04-25

Completion date

Unknown

Last updated

2021-12-13

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

Experimental group:Use the turning device to adjust the critically ill patient to the prone position

Control group:Routine turning method

Eligibility

Sex/Gender

All

Age

18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. According to the Berlin definition, it meets the diagnostic criteria of ARDS; 2. The patients who receiving tracheal intubation and mechanical ventilation less than 48 hours; 3. Aged 18 to 75 years.

Exclusion criteria

Exclusion criteria: 1. Unstable fracture of the spine; 2. Pregnant women; 3. The estimated time of invasive mechanical ventilation is less than 48 hours; 4. Intracranial hypertension; severe COPD patients; dying patients.

Design outcomes

Primary

Measure	Time frame
Number of staff;	—

Secondary

Measure	Time frame
Respiratory complications;Circulatory complications;Pipeline complications;Cutaneous complications;The use of sedatives;	—

Countries

China

Contacts

Public ContactShuai Weizheng

The Sixth Medical Center of PLA General Hospital

icuswz@163.com+86 18600310671

Outcome results

None listed

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