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Citrate Anticoagulation for Postdilution Hemofiltration

Citrate Anticoagulation for Postdilution Hemofiltration

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03969966
Acronym
CIPOHA
Enrollment
100
Registered
2019-05-31
Start date
2019-01-14
Completion date
2021-07-31
Last updated
2020-05-11

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

Conditions

Acute Kidney Injury, Critical Illness

Brief summary

This study evaluates a protocol for regional citrate anticoagulation in critically ill patients with acute kidney injury who are treated with continuous veno-venous haemofiltration in postdilution mode.

Detailed description

Acute kidney injury (AKI) requiring continuous renal replacement therapy (CCRT occurs in approx. 15 % of all intensive care patients. A sustained and prolonged filter running time is required to deliver an effective dialysis dose. This requires effective anticoagulation. Today, regional citrate anticoagulation (RCA) is preferred over systemic anticoagulation because of prolonged filter lifetimes and less adverse effects. We here study prospectively patients with AKI who are treated with continuous veno-venous haemofiltration using an RCA protocol. We will evaluate all parameters of CRRT including filter running times, delivered dialysis dose, causes for treatment interruption and control of pH and electrolytes.

Interventions

OTHERrenal replacement therapy as clinically indicated

Continuous renal replacement therapy

Sponsors

Diamed GmbH, Cologne, Germany
CollaboratorUNKNOWN
Heinrich-Heine University, Duesseldorf
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum

Inclusion criteria

* acute kidney injury * critical illness and treatment at ICU

Exclusion criteria

* age \< 18 years * pregnancy or breast feeding * severe lactate acidosis ( \> 10 mmol/l) for longer than 6 hours and pH \< 7.2

Design outcomes

Primary

MeasureTime frameDescription
Filter running time72 hoursFilterlifetime with regional citrate anticoagulation for haemofiltration

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 7, 2026