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Clinical efficacy of HA380 cytokine adsorption therapy in patients undergoing cardiac surgery for infective endocarditis: a prospective study

Clinical efficacy of HA380 cytokine adsorption therapy in patients undergoing cardiac surgery for infective endocarditis: a prospective study

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200063699
Enrollment
Unknown
Registered
2022-09-15
Start date
2022-10-01
Completion date
Unknown
Last updated
2023-04-17

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

Conditions

Infective endocarditis

Interventions

Control Group:Surgical treatment of infective endocarditis
Treatment group:Surgical treatment of infective endocarditis+HA380 treatment

Sponsors

Drum Tower Hospital, School of Medicine, Nanjing University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1) No restriction on gender, age over 18; 2) Infective endocarditis (IE), which meets the modified Duke diagnostic criteria and has surgical indications according to the 2015 European Society of Cardiology IE management guidelines; 3) Signed informed consent.

Exclusion criteria

Exclusion criteria: 1) Low-risk patients with EuroScore II =3 for cardiac surgery; 2) Currently participating in other clinical trials; 3) Patients allergic to hemoperfusion, filter and anticoagulant; 4) Patients who were pregnant or suspected of being pregnant or breastfeeding at the time of inclusion; 5) Patients with malignant tumor or connective tissue disease; 6) Patients with rheumatic immune diseases; 7) Infective endocarditis with systemic immune response; 8) Liver and kidney diseases before surgery. 9) The written consent of the patient or client cannot be obtained.

Design outcomes

Primary

MeasureTime frame
Perioperative mortality;Rate of secondary thoracotomy;postoperative kidney failure;paraplegia;Stroke/cerebrovascular accident;Low cardiac output syndrome;Retracheal intubation;Severe liver dysfunction;ECMO;multiple organ dysfunction syndrome;

Secondary

MeasureTime frame
Inflammatory factor;SOFA score;24 hours discharge;postoperative acute kidney injury;postoperative respiratory failure;postoperative delirium;postoperative liver injury;postoperative myocardial infarction;postoperative Mechanical ventilation time;

Countries

China

Contacts

Public ContactLiu Chang

Drum Tower Hospital, School of Medicine, Nanjing University

liuchang5927@163.com13357832795

Outcome results

None listed

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