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Safety and efficacy of regional citrate compared to non-heparin as anticoagulation in conventional dialysis of patients with a high risk of bleeding

Safety and efficacy of regional citrate compared to non-heparin as anticoagulation in conventional dialysis of patients with a high risk of bleeding

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900027928
Enrollment
Unknown
Registered
2019-12-04
Start date
2019-12-22
Completion date
Unknown
Last updated
2019-12-10

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

Conditions

kidney failure

Interventions

Group 2:Anticoagulation with citric acid
Group 1:Heparin anticoagulation

Sponsors

CQ Southwest Hospital Nephrology Department
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18 to 70 years old, male or female; 2. Acute or chronic renal failure requiring hemodialysis; 3. Voluntarily participate in this clinical trial and sign the informed consent form; 4. Risk of bleeding or active bleeding.

Exclusion criteria

Exclusion criteria: 1. Recent (7 days) use of antiplatelet drugs and/or use of anticoagulant drugs (other than anticoagulant drugs necessary for hemodialysis); 2. Patients with severe hypoxemia; 3. Patients with refractory hypocalcemia; 4. Patients with severe alkalosis that cannot be corrected; 5. Anemia patients with hemoglobin less than 50g/L; 6. Abnormal liver function (ALT and/or AST > upper limit of 1.5 times), severe hematologic disease, malignant tumor or other underlying disease; 7. Alcohol or substance abusers; 8. Have mental illness cannot cooperate; 9. Allergic constitution, known to be allergic to the test drug (sodium citrate) and its excipients or heparin Pregnant, recently pregnant, nursing women; 10. Participants in other clinical trials in the past 1 month; 11. The researchers concluded that there were other conditions that were not suitable for inclusion.

Design outcomes

Primary

MeasureTime frame
analysis of blood gas;electrolyte;ACT;

Secondary

MeasureTime frame
urine routine;blood routine;liver function;coagulation function;

Countries

China

Contacts

Public ContactPan Xie

CQ Southwest Hospital Nephrology Department

13485545@qq.com+86 18623199726

Outcome results

None listed

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