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Safety and Efficacy of Regional Citrate Anticoagulation During Sustained Low-Efficiency Dialysis

Safety and Efficacy of Regional Citrate Anticoagulation During Sustained Low-Efficiency Dialysis

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-11001582
Enrollment
Unknown
Registered
2011-09-13
Start date
2011-01-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

acute/chronic renal failure

Interventions

A:SLED with calcium-free dialysate and citrate
B:SLED with calcium-containing dialysate and heparin

Sponsors

Department of nephrology, West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: With the need of renal replacement therapy because of acute/chronic renal failureAcute renal failure (ARF): 1. ARF combined with hyperkalemia, acidosis, pneumonedema; 2. ARF combined with heart failure; 3. ARF combined with encephaledema; 4. ARF combined with high catabolism; 5. ARF combined with ARDS; 6. Hemodynamic instability; 7. After cardiosurgery; 8. SepsisChronic renal failure under maintenance hemodialysis: (1) acute pneumonedema; (2) Hemodynamic instability; (3) severe edema.

Exclusion criteria

Exclusion criteria: 1. Less than 18 years old; 2. Hypercalemia (serum total calcium > 2.6mmol/L); 3. Citrate acid can't be metabolized efficiently because of severe hyoxemia, hepatic renal failure and muscle hypoperfusion; 4. With the need of additional anticoagulant or hemostasis drug in the treatment; 5. HIV infection; 6. Pregnancy, organ transplantation recipient within 1 year or cachexia; 7. Allergy of cardiopulmonary circulation, anticoagulant or blood purification equipments; 8. Cannot undergo blood purification treatment because of other diseases or having severe complications during treatment; 9. Cannot cooperate effectively during treatment; 10. Involved in other clinical trails; 11. Considered not suitable for the trail by doctors (at least 2 attendings).

Design outcomes

Primary

MeasureTime frame
Coagulation indexes (APTT, PT, PLT);Survival rate of patients in 30 and 60 days;iCa2+ of peripheral blood and blood gas in 0, 2, 6 h;Trans-membrane, arterial and venous pressure;Lifetime of dialyzer and pipeline;Blood-clotting degree of dialyzer (I, II, III, IV);Adverse reactions (systemic and local's hemorrhage, hypocalcemia/ hypercalcemia, acidosis/ alkalosis;Citrate concentration in 0, 2, 6hours (Venous, arterious);Value of PH and BE in 0, 2, 6 hours;The relationship between Citrate concentration and related PH value and iCa2+;

Countries

China

Contacts

Public ContactPing Fu,Ling Zhang
fupinghx@163.com+86 18980601201

Outcome results

None listed

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