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Objective to compare the anticoagulant efficacy and safety of simplified citric acid anticoagulation and conventional citrate anticoagulation in hemodialysis patients: a cross controlled clinical trial

Objective to compare the anticoagulant efficacy and safety of simplified citric acid anticoagulation and conventional citrate anticoagulation in hemodialysis patients: a cross controlled clinical trial

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900024978
Enrollment
Unknown
Registered
2019-08-05
Start date
2019-08-04
Completion date
Unknown
Last updated
2019-08-27

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

Conditions

Hemodialysis

Interventions

1:phase I: low dose citrate anticoagulation, 3 times
phase II: normal dose citrate anticoagulation, 3 times.
2:phase I: normal dose citrate anticoagulation, 3 times
phase II: low dose citrate anticoagulation, 3 times.

Sponsors

Department of Nephrology, Sichuan Academy of Medical Science and Sichuan Provincial People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1) Sign the written informed consent form. 2) Patients between the ages of 18 and 75 are not limited to men and women. 3) Maintenance hemodialysis patients (dialysis over 3 months), dialysis 3 times a week, of which at least 2 times a week for general hemodialysis. 4) Patients with stable blood flow velocity during dialysis and greater than 180 mL/min. The blood flow velocity during the dialysis was stable and was greater than 180 mL/min. 5) There is a risk of bleeding and it is not possible to use heparin anticoagulation patients.

Exclusion criteria

Exclusion criteria: 1) Respiratory failure. 2) Liver dysfunction, serum ALT and AST are more than 2 times the upper limit of normal. 3) Patients with congenital heart disease, arrhythmia, heart failure and other serious cardiovascular diseases. 4) Patients who use other anticoagulant drugs at the same time (including heparin, low molecular weight heparin, direct anticoagulant preparation, warfarin, etc.). 5) Female patients who are pregnant, breast-feeding, or unwilling to take contraception. 6) Patients who have participated in other clinical trials within the first three months of enrollment. 7) The investigator judges that the patient's condition is not suitable for participation in this experimental study.

Design outcomes

Primary

MeasureTime frame
Blood gas analysis;Complete dialysis ratio;Complications;Coagulation grading;

Countries

China

Contacts

Public ContactHong Daqing; Deng Fei

Sichuan Academy of Medical Sciences & Sichuan Provincial People's Hospital

hongdaqing11@126.com+86 18981838230

Outcome results

None listed

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