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In vitro blood compatibility assessment research of novel blood-contacting materials

In vitro blood compatibility assessment research of novel blood-contacting materials

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400083626
Enrollment
Unknown
Registered
2024-04-29
Start date
2024-04-30
Completion date
Unknown
Last updated
2024-05-06

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

Conditions

Extracorporeal Blood Compatibility Study

Interventions

Observation group:N/A

Sponsors

Nephrology Department, West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
22 Years to 28 Years

Inclusion criteria

Inclusion criteria: 1. Adults aged 22-28 years (inclusive of 22 and 28), of any gender. 2. Capable of understanding the purpose of the trial, willing to participate voluntarily, and able to sign an informed consent form. 3. Normal blood pressure, blood lipid levels, blood glucose levels, and body temperature. 4. No immunodeficiency disorders or infectious diseases. 5. Normal coagulation function and no intake of anticoagulant medications in the past 4 weeks.

Exclusion criteria

Exclusion criteria: 1. Under 22 years old or over 28 years old. 2. Mentally abnormal or with uncorrected consciousness disorders, unable to cooperate with blood collection. 3. Symptoms of hypertension, hyperglycemia, hyperlipidemia, or abnormal body temperature. 4. Immunodeficiency disorders or infectious diseases. 5. Severe coagulation dysfunction or failure to stop oral anticoagulants for the required duration. 6. Needle phobia or syncope. 7. Patients with anemia.

Design outcomes

Primary

MeasureTime frame
Hemolysis rate;Blood cell count;Clotting time;Coagulation factor activity;Plasma proteomics;Complement protein concentration;

Secondary

MeasureTime frame
Platelet morphology;Level of neutrophil activation;

Countries

China

Contacts

Public ContactLi Yupei

West China Hospital of Sichuan University

sculyp@163.com+86 186 2821 0140

Outcome results

None listed

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