Status:
RECRUITING
Safety Evaluation of Prismocitrate 18 in Patients Receiving CRRT
Lead Sponsor:
Vantive Health LLC
Collaborating Sponsors:
Baxter Healthcare Corporation
Conditions:
Regional Citrate Anticoagulation (RCA)
Continuous Renal Replacement Therapy (CRRT)
Eligibility:
All Genders
18+ years
Phase:
PHASE3
Brief Summary
Prismocitrate 18 is a continuous renal replacement therapy (CRRT) solution to be used as a renal replacement solution and as an anticoagulant to prevent blood clotting in the extracorporeal circuit. T...
Eligibility Criteria
Inclusion
- Patients must be ≥18 years of age
- Patients who are candidates for CRRT
- Patients expected to survive for at least 24 hours
- Patients with a contraindication to heparin or an increased risk of hemorrhage
- Patient and/or legally-authorized representative has signed a written informed consent form (ICF) per 21 CFR Part 50.55(e)
Exclusion
- Patients with a known allergy to citrate or who have ever experienced an adverse reaction associated with citrate products, including patients with a prior history of citrate toxicity
- Patients with acute liver failure, defined by the occurrence of encephalopathy and hepatic synthetic dysfunction within 26 weeks of the first symptoms of liver disease and without evidence of chronic liver disease
- Patients with acute-on-chronic liver failure characterized by acute decompensation of cirrhosis and a Child-Pugh Liver Failure Score \>10
- Patients with refractory shock and associated lactic acidosis (lactate \>4 mmol/L)
- Patients with a systemic ionized calcium concentration outside the normal physiologic range (1.0 - 1.3 mmol/L), or outside of the laboratory reference range (Note: It is acceptable to provide calcium supplementation or treatment for hypercalcemia to achieve a normal physiologic range prior to therapy initiation)
- Female patients of childbearing potential who are pregnant or breastfeeding. (Note: All female patients, who have not undergone a hysterectomy, bilateral oophorectomy with or without hysterectomy, or has medically documented ovarian failure before study Screening must have a negative serum beta human chorionic gonadotropic \[B-hCG\] pregnancy test at Screening)
- Patients who are currently participating in another interventional clinical study
Key Trial Info
Start Date :
July 12 2024
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
December 1 2026
Estimated Enrollment :
40 Patients enrolled
Trial Details
Trial ID
NCT05399537
Start Date
July 12 2024
End Date
December 1 2026
Last Update
December 16 2025
Active Locations (14)
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1
University of Alabama at Birmingham/UAB
Birmingham, Alabama, United States, 35294-0007
2
University of Southern California (USC) / Keck Hospital
Los Angeles, California, United States, 90033
3
University of California Los Angeles
Los Angeles, California, United States, 90095
4
University of Miami
Miami, Florida, United States, 33136