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Clinical Trial

Safety Evaluation of Prismocitrate 18 in Patients Receiving CRRT

NCT: NCT05399537 · RECRUITING

NCT IDNCT05399537
StatusRECRUITING
Start Date2024-07-12
Completion2026-12

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. The delivery of CRRT therapy is provided by the PrisMax System which includes regional citrate anticoagulation (RCA) software to facilitate citrate and calcium compensation prescription. The objectives of this study are: 1) to confirm the safety of Prismocitrate 18 in patients receiving CRRT using continuous venovenous hemodiafiltration (CVVHDF) or continuous venovenous hemofiltration (CVVH) and 2) to observe that the software and interface for the PrisMax System Version 3.x with calcium line accessory allows for implementation of regional citrate anticoagulation (RCA) (citrate and calcium dosing) during CRRT with Prismocitrate 18 and intended prescription. The study period of the patient's CRRT will be up to 10 days.

Frequently Asked Questions

What is Safety Evaluation of Prismocitrate 18 in Patients Receiving CRRT?

Safety Evaluation of Prismocitrate 18 in Patients Receiving CRRT is a clinical trial registered under NCT05399537. Current status: RECRUITING.

What is the status of NCT05399537?

The current status of NCT05399537 (Safety Evaluation of Prismocitrate 18 in Patients Receiving CRRT) is: RECRUITING.

When did Safety Evaluation of Prismocitrate 18 in Patients Receiving CRRT start?

Safety Evaluation of Prismocitrate 18 in Patients Receiving CRRT started on 2024-07-12.

Official Source

View on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.