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Clinical Trial Summary

Multicentre, open, prospective and interventional study investigating the CardioRenal device in capillary blood of patients.It will be conducted at multiple investigational sites.


Clinical Trial Description

Objectives are to assess the quantitative accuracy in freshly collected whole capillary blood from patients and healthy volunteers and to evaluate user proficiency. In order to gather a wide range of K+ concentrations, the study will be conducted both on patients or healthy volunteers and on dialysis patients. The study includes 2 phases (calibration phase and comparison phase) where blood samples (capillary and venous) will be collected.Blood is taken from the subject by trained specialist staff. During the comparison phase, the subjects will be equipped with CardioRenal device and trained to do the self-test. A subject's participation in this study (both calibration and validation phase) will consist of two interventional visits for hemodialysis patients and three interventional visits for other subjects. ;


Study Design


NCT number NCT05975632
Study type Interventional
Source CardioRenal
Contact Maurice BERENGER, PhD
Phone +33613903869
Email support@cardio-renal.com
Status Recruiting
Phase N/A
Start date August 2, 2023
Completion date March 2024