Kidney Disease Clinical Trial
Official title:
Designing a Bayesian Model of the Plasma Clearance of Calcium Edetate de Sodium, With a Limited Sampling Strategy for the Calculation of Glomerular Filtration Rate (GFR) and Validity Assessment Compared to the Renal Clearance of Inulin : DFGBay
Diagnosis of patients with renal insufficiency and recommendations for medical treatment of
patients who suffer from chronic renal failure are based on the different stages of
Glomerular Filtration Rate (GFR). Many formulas exist to assess GFR. However these formulas
are unreliable in many clinical situations (old people, obese patients…). Methods for
measuring GFR using exogenous tracers exist: Inulin and 51Cr-EDTA are historical reference
tracers. Renal clearance of Inulin is the gold standard. However, using these methods is
restricted to specialized services because it is long and expensive.
There is no medical data for the use of Calcium edetate de sodium as a tracer to assess GFR.
Calcium edetate de sodium is a treatment for lead intoxication. The extension of use as a
tracer comes from its exclusive elimination by glomerular filtration.
Plasma and renal clearance of Calcium edetate de sodium and Inulin will be measured for every
included patient during a hospital day care (First visit V1). For transplanted patients,
plasma clearance of Calcium edetate de sodium will be repeated within one week (more or less
48hours) during annual medical check-up of renal transplantation (Second visit V2).
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