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| ID | Type | Description | Link |
|---|---|---|---|
| 101125504 | Other Grant/Funding Number | European Research Council | |
| NL-005327 | Other Identifier | Onderzoeksportaal | |
| NL87576.078.24 | Other Identifier | Toetsing Online |
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| Name | Class |
|---|---|
| European Research Council | OTHER |
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The goal of this clinical trial is to predict the progression of chronic kidney disease by diuretic testing in patients with chronic kidney disease. The main questions it aims to answer are:
Does a worse result of a diuretic test predict the progression of chronic kidney disease?
If there is a comparison group: Researchers will compare the diuretic test in patients with chronic kidney disease to healthy participants to see if the results are different in a healthy kidney.
Participants will undergo diuretic testing. This involves the administration of bumetanide and hydrochlorothiazide with subsequent blood and urine collections.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Diuretic Group | Experimental | Administration of diuretics on the test day |
|
| Time control group | No Intervention | No diuretics will be administered |
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Diuretic Testing | Diagnostic Test | The administration of hydrochlorothiazide and bumetanide is used to stimulate and assess tubular function. |
|
| Measure | Description | Time Frame |
|---|---|---|
| Progression of Chronic Kidney Disease | This composite outcome consists of the reduction of kidney function of 30% measured as creatinine-based estimated glomerular filtration rate (eGFR) using the chronic kidney disease epidemiology collaboration (CKD-EPI) 2021 formula or the initiation of kidney replacement therapy (dialysis or kidney transplantation) | 3 years |
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Inclusion Criteria for CKD subjects:
Inclusion Criteria for Healthy subjects:
• eGFR within the expected range for age (a decline of 1 ml/min/1.73 m2 per year starting from age 40 is considered the normal age-related decline in kidney function
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Sebastian B Beckmann, MD | Contact | +31 6 39022349 | s.beckmann@erasmusmc.nl |
| Name | Affiliation | Role |
|---|---|---|
| Ewout J. Hoorn, MD, PhD | Erasmus Medical Center | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Erasmus MC | Recruiting | Rotterdam | South Holland | 3015GD | Netherlands |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 17699451 | Background | Colussi G, Bettinelli A, Tedeschi S, De Ferrari ME, Syren ML, Borsa N, Mattiello C, Casari G, Bianchetti MG. A thiazide test for the diagnosis of renal tubular hypokalemic disorders. Clin J Am Soc Nephrol. 2007 May;2(3):454-60. doi: 10.2215/CJN.02950906. Epub 2007 Mar 14. | |
| 24053972 | Background | Chawla LS, Davison DL, Brasha-Mitchell E, Koyner JL, Arthur JM, Shaw AD, Tumlin JA, Trevino SA, Kimmel PL, Seneff MG. Development and standardization of a furosemide stress test to predict the severity of acute kidney injury. Crit Care. 2013 Sep 20;17(5):R207. doi: 10.1186/cc13015. |
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| ID | Term |
|---|---|
| D051436 | Renal Insufficiency, Chronic |
| D018450 | Disease Progression |
| ID | Term |
|---|---|
| D051437 | Renal Insufficiency |
| D007674 | Kidney Diseases |
| D014570 | Urologic Diseases |
| D052776 | Female Urogenital Diseases |
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| 11231365 | Background | Rodriguez-Iturbe B, Herrera J, Marin C, Manalich R. Tubular stress test detects subclinical reduction in renal functioning mass. Kidney Int. 2001 Mar;59(3):1094-102. doi: 10.1046/j.1523-1755.2001.0590031094.x. |
| D005261 |
| Female Urogenital Diseases and Pregnancy Complications |
| D000091642 | Urogenital Diseases |
| D052801 | Male Urogenital Diseases |
| D002908 | Chronic Disease |
| D020969 | Disease Attributes |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |