Application of wearable ECMO in severe ARDS

Status

Active, not recruiting

Phases

Early Phase 1

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR2100046240

Enrollment

Unknown

Registered

2021-05-12

Start date

2021-07-01

Completion date

Unknown

Last updated

2021-12-21

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

Conditions

Severe Acute Respiratory Distress Syndrome

Interventions

Simple extracorporeal membrane oxygenation group:None

Conventional extracorporeal membrane oxygenation group:None

Eligibility

Sex/Gender

All

Age

18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Severe ARDS (Berlin standard), which could not be improved by conventional treatment, and the duration of mechanical ventilation was less than 7 days; 2. Aged 18 to 70 years; 3. Sign informed consent.

Exclusion criteria

Exclusion criteria: 1. Irreversible brain injury; 2. Uncontrollable active bleeding; 3. Terminal stage of malignant tumor or chronic disease.

Design outcomes

Primary

Measure	Time frame
Mortality;	—

Secondary

Measure	Time frame
Thrombotic events;Bleeding events;Infection events;	—

Countries

China

Contacts

Public ContactRen Hongsheng

Provincial Hospital Affiliated to Shandong First Medical University

chunancy@163.com+86 531 68777920

Outcome results

None listed

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