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Application and evaluation of dexmedetomidine combined with sedation in the comfortable medical management of critically ill patients with ECMO support

Application and evaluation of dexmedetomidine combined with sedation in the comfortable medical management of critically ill patients with ECMO support

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100050917
Enrollment
Unknown
Registered
2021-09-08
Start date
2021-09-01
Completion date
Unknown
Last updated
2022-05-09

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

Conditions

Cardiopulmonary failure

Interventions

Traditional sedation group:Midazolam/Propofol
Comfortable sedation group:Dexmedetomidine combined with sedation titration

Sponsors

Qilu Hospital of Shandong University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1. Patients with severe and reversible cardiopulmonary failure requiring ECMO support; 2. Aged 18-75 years; 3. Patients or their entrusted agent sign the informed consent.

Exclusion criteria

Exclusion criteria: 1. Heparin-induced thrombocytopenia (HIT); 2. Patients who have been confirmed or suspected to be accompanied by nerve injury; 3. Pregnant patients, Alzheimer's disease, or psychiatric diseases; 4. Serious primary diseases affecting survival: multiple unresectable malignant tumors, blood diseases and HIV, etc.; 5. Burns, drug overdose or poisoning, acute liver failure; 6. The need for continuous use of neuromuscular blocking agents; 7. Patients who have been determined by the competent doctor to be unsuitable for inclusion in the group.

Design outcomes

Primary

MeasureTime frame
Richmond agitation sedation scale;Cumulative amount of sedative and analgesic drugs used;

Countries

China

Contacts

Public ContactGuo Haipeng

Qilu Hospital of Shandong University

haipeng198334@163.com+86 531 82165811

Outcome results

None listed

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