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The effect of HA380 hemoperfusion device on postoperative delirium in elderly patients undergoing cardiac surgery: a prospective randomized controlled trial

The effect of HA380 hemoperfusion device on postoperative delirium in elderly patients undergoing cardiac surgery: a prospective randomized controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400085575
Enrollment
Unknown
Registered
2024-06-12
Start date
2022-11-01
Completion date
Unknown
Last updated
2024-07-08

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

Conditions

delirium

Interventions

hemoperfusion group:Using HA380 hemoperfusion device during cardiopulmonary bypass
control group:Using conventional cardiopulmonary bypass without HA380 hemoperfusion.

Sponsors

Fujian Provincial Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to 85 Years

Inclusion criteria

Inclusion criteria: ?Patients older than 65 years old.?Elective cardiopulmonary bypass for combined valve replacement/plasty, ascending aortic aneurysm surgery, etc., with an expected CPB time of more than 2 hours.?Volunteer to participate in this study and sign informed consent form.

Exclusion criteria

Exclusion criteria: ?Patients with cognitive disorders, Alzheimer's disease, anxiety and other mental disorders.?Patients with liver diseases, renal insufficiency, or cerebrovascular diseases.?Using psychotropic drugs or other drugs that interfere the evaluation of delirium and cognitive function.?Patients with serious problem in hearing and understanding, or who are unable to cooperate and provide informed consent.

Design outcomes

Primary

MeasureTime frame
Postoperative delirium;

Secondary

MeasureTime frame
TNF-a;IL-6;IL-10;S100ß protein;NSE;Procalcitonin (PCT);C-reactive protein (CPR);Alanine transaminase (ALT);Aspartate transaminase (AST);Creatinine (Cr);Blood gas parameters;Length of hospital stay;Length of ICU hospital stay;Duration of mechanical ventilation;Postoperative complications;

Countries

China

Contacts

Public ContactLihua Lei

Fujian Provincial Hospital

lei_234@163.com+86 137 0504 5270

Outcome results

None listed

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