Tubular stress test detects subclinical reduction in renal functioning mass.
B Rodríguez-Iturbe, J Herrera, C Marín...
https://pubmed.ncbi.nlm.nih.gov/11231365/Actively Recruiting
Led by Erasmus Medical Center · Updated on 2025-08-07
86
Participants Needed
1
Research Sites
N/A
Total Duration
Researchers are investigating how diuretic testing can predict the progression of chronic kidney disease CKD. The study focuses on whether poorer results from this test indicate faster worsening of CKD. It also compares the test results between patients with CKD and healthy individuals to understand differences in kidney function. Participants are randomly assigned to one of two groups one group receives diuretics hydrochlorothiazide and bumetanide to stimulate kidney tubular function, while the other group does not receive diuretics. Blood and urine samples are collected after administration to assess kidney response. This interventional study involves a test day where diuretics are given and monitoring occurs. During the study, participants will undergo diuretic testing with blood and urine collections to evaluate kidney function. Researchers will monitor the progression of CKD over three years as the primary outcome. Safety and adherence will be observed, and participants health will be assessed throughout the study period. The total involvement includes initial testing and long-term follow-up to measure disease progression.
CONDITIONS
Diuretic Testing in Chronic Kidney Disease
S
Sebastian B Beckmann, MD
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Erasmus Medical Center
Lead Sponsor
European Research Council
Collaborating Sponsor
You may qualify if you...
You will not qualify if you...
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 1 day
Participants undergo diuretic testing with administration of hydrochlorothiazide and bumetanide to stimulate and assess kidney tubular function.
1 visit (in-person) on the test day
Duration - 3 years
Participants are monitored for progression of chronic kidney disease over time.
Periodic visits as per study protocol
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
DIAGNOSTIC
Number of Arms
2
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B Rodríguez-Iturbe, J Herrera, C Marín...
https://pubmed.ncbi.nlm.nih.gov/11231365/Lakhmir S Chawla, Danielle L Davison, Ermira Brasha-Mitchell...
https://pubmed.ncbi.nlm.nih.gov/24053972/Giacomo Colussi, Alberto Bettinelli, Silvana Tedeschi...
https://pubmed.ncbi.nlm.nih.gov/17699451/Erasmus Medical Center
Lead Sponsor
European Research Council
Collaborating Sponsor