Evaluation of the safety and effectiveness of long-term prone position therapy in patients with ARDS

Status

Recruiting

Phases

Early Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR2300075887

Enrollment

Unknown

Registered

2023-09-19

Start date

2023-09-20

Completion date

Unknown

Last updated

2023-09-26

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

Conditions

ARDS

Interventions

Prone group:NA

Supine group:NA

Eligibility

Sex/Gender

All

Age

18 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1. ARDS patients with P/F index less than 200mmHg; 2. Patients over 18 years old; 3. Those who agree to participate in this study and are willing to sign an informed consent form.

Exclusion criteria

Exclusion criteria: The patient has a relative contraindication of prone position, such as after spinal surgery, pregnancy, and intolerance of prone position

Design outcomes

Primary

Measure	Time frame
ratio of arterial oxygen partial pressure to fractional inspired oxygen;30 day mortality ;Mechanical ventilation time;	—

Secondary

Measure	Time frame
Braden pressure ulcer score;NPUAP pressure ulcer classification;Diameter of optic nerve sheath;Intraocular pressure values;	—

Countries

China

Contacts

Public ContactZheng Xia

The First Affiliated Hospital of Zhejiang University School of Medicine

zxicu@zju.edu.cn+86 139 5817 4688

Outcome results

None listed

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