A Prospective, Observational Study to Evaluate the Safety and Feasibility of Continuous Renal Replacement Therapy With Regional Citrate Anticoagulation in a Cohort Critical Ill Patients With Acute Kidney Injury and Presumed Absent Citrate Metabolism
Starting soon
Conditions studied: Acute Kidney Injury
In brief
Use of regional citrate anticoagulation in an at risk population with decreased citrate metabolism. This study assesses the feasibility and safety of regional citrate anticoagulation in this population.
Key facts
- Study ID
- NCT07751874
- Run by
- University Hospital, Antwerp
- People needed
- 50
- Starts
- 2026-10-15
- Expected to finish
- 2028-07-01
- Last updated by the study team
- 2026-08-07
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Need for renal replacement therapy in the ICU with any of the following criteria:
- anticipation of severely impaired citrate metabolism (serum lactate ≥ 5 mmol/l in patients with shock or requirement of a dextrose drip to prevent hypoglycemia or spontaneous INR > 3 and/or requirement of fresh frozen plasma to maintain INR < 3 in patients with cirrhosis or acute liver failure or acute on chronic liver failure)
- development of citrate toxicity under CRRT with RCA due to worsening citrate metabolism
You may not qualify if…
- Pregnancy
- A known hypersensitivity to citrate compounds
- Refusal of informed consent
Where it is running
- Antwerp University Hospital — Edegem, Antwerp, Belgium
Full record on ClinicalTrials.gov
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