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The clinical research plan of citrate dialysate in hemodialysis anticoagulation effect

The clinical research plan of citrate dialysate in hemodialysis anticoagulation effect

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100047224
Enrollment
Unknown
Registered
2021-06-11
Start date
2021-07-01
Completion date
Unknown
Last updated
2022-02-01

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

Conditions

Hemodialysis

Interventions

Experimental group:Citrate dialysate dialysis
Control group:Acetate dialysate

Sponsors

West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Patients who are currently undergoing hemodialysis treatment, aged 18 years and above; 2.The vascular access is unobstructed, and the blood flow is >= 200ml/min; 3.Indications for heparin-free dialysis (mainly refers to recent surgery, internal bleeding); 4.Normal patients who are able to communicate both verbally and in writing; 5.Voluntarily participate in this study and sign an informed consent form.

Exclusion criteria

Exclusion criteria: 1. Hypocalcemia; 2. Hypersensitivity to citric acid; 3. Liver dysfunction (ALT or AST levels more than twice the upper limit); 4. Abnormal coagulation indicators: activated partial thromboplastin time (APTT) is significantly prolonged (10 more than normal controls) Seconds or more), platelets (PLT) < 50x10^9/L; 5. Anticoagulant drugs or continuous antithrombotic therapy have been used within 24 hours before treatment; 6. Malignant tumors.

Design outcomes

Primary

MeasureTime frame
Coagulation conditions;

Secondary

MeasureTime frame
adverse reaction;

Countries

China

Contacts

Public ContactChen Lin

West China Hospital, Sichuan University

clhxxuetou@163.com+86 18980601205

Outcome results

None listed

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