- Trials with a EudraCT protocol (54)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (2)
54 result(s) found for: Nephrosis.
Displaying page 1 of 3.
EudraCT Number: 2009-011406-42 | Sponsor Protocol Number: P071221 | Start Date*: 2010-02-02 | |||||||||||
Sponsor Name:ASSISTANCE PUBLIQUE - HOPITAUX DE PARIS (AP-HP) | |||||||||||||
Full Title: Etude randomisée prospective comparant l'effet du cyclophosphamide et du mycophénolate chez les enfants atteints de néphrose corticodépendante | |||||||||||||
Medical condition: enfants atteints de néphrose corticodépendante | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-001206-16 | Sponsor Protocol Number: 121934 | Start Date*: 2017-09-15 | ||||||||||||||||
Sponsor Name:Aarhus University hospital | ||||||||||||||||||
Full Title: Treatment of primary minimal change nephropathy. A randomized, open-labeled, non-inferiotiry study on prednisolone and vitamin D | ||||||||||||||||||
Medical condition: Minimal Change Nephropathy | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-004301-41 | Sponsor Protocol Number: P170404J | Start Date*: 2018-10-15 | |||||||||||
Sponsor Name:ASSISTANCE PUBLIQUE-HOPITAUX DE PARIS [...] | |||||||||||||
Full Title: FURosemide Stress Test to predict need of Renal Replacement THERapy in Ischemic Acute Tubular Necrosis in Intensive Care Units | |||||||||||||
Medical condition: FURosemide Stress Test to predict need of Renal Replacement THERapy in Ischemic Acute Tubular Necrosis in Intensive Care Units | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-006750-17 | Sponsor Protocol Number: NEMO | Start Date*: 2009-04-14 | |||||||||||||||||||||
Sponsor Name:IST. DI RICERCHE FARMACOLOG. M. NEGRI | |||||||||||||||||||||||
Full Title: A prospective, sequential study to assess the efficacy of rituximab therapy in maintaining remission of nephrotic syndrome after steroid and immunosuppressive therapy withdrawal in patients with st... | |||||||||||||||||||||||
Medical condition: Nephrotic Syndrome secondary to minimal change disease (MCD) or idiopathic focal and segmental glomerulosclerosis (FSGS. | |||||||||||||||||||||||
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Population Age: Adolescents, Under 18, Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: IT (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2006-004467-65 | Sponsor Protocol Number: DNTx | Start Date*: 2007-04-24 | |||||||||||
Sponsor Name:Technical University Dresden | |||||||||||||
Full Title: Influence of pioglitazone for renal transplant function in diabetics | |||||||||||||
Medical condition: nephropathy after renal transplantation in patients with type 2 diabetes | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-000786-32 | Sponsor Protocol Number: SPP301CRD21 | Start Date*: 2008-06-17 | |||||||||||
Sponsor Name:Speedel Pharma Ltd | |||||||||||||
Full Title: A Randomised, Double-blind, Placebo-Controlled, Dose-ranging, Parallel Design Study to Evaluate the Efficacy and Safety of the Endothelin Antagonist Avosentan in Patients With Diabetic Kidney Disease | |||||||||||||
Medical condition: Diabetic kidney disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SK (Completed) BE (Completed) LV (Prematurely Ended) CZ (Prematurely Ended) HU (Prematurely Ended) DE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-000722-19 | Sponsor Protocol Number: M12-919 | Start Date*: 2016-10-24 | |||||||||||
Sponsor Name:AbbVie Deutschland GmbH & Co. KG | |||||||||||||
Full Title: A Multicenter, Single-Arm Study of the Effects of Atrasentan on Spermatogenesis and Testicular Function | |||||||||||||
Medical condition: Diabetic Nephropathy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: DE (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-003053-37 | Sponsor Protocol Number: 21952 | Start Date*: 2021-11-05 | |||||||||||
Sponsor Name:Bayer AG | |||||||||||||
Full Title: A non-blinded retrospective biomarker add-on study to FIGARO-DKD for Bioprofiling the pharMacodynamic response to finerenone in FIGARO-DKD subjects (FIGARO-BM) | |||||||||||||
Medical condition: Type II Diabetes Mellitus and Diabetic Kidney Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BG (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-000087-12 | Sponsor Protocol Number: DXV406 | Start Date*: 2005-08-16 | |||||||||||
Sponsor Name:Amersham Health S.A. (parte de GE Healthcare Ltd y sus filiales) | |||||||||||||
Full Title: Estudio multicéntrico, aleatorizado, doble ciego, de grupos paralelos, en fase IV, para comparar los efectos renales del medio de contraste no iónico isosmolar, iodixanol 320 mg I/ml (VisipaqueTM),... | |||||||||||||
Medical condition: Subjects with a combination of diabetes mellitus (type I or II), and impaired renal function. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-005482-12 | Sponsor Protocol Number: GLP-1-2012-01 | Start Date*: 2013-04-15 | |||||||||||
Sponsor Name:University College Dublin | |||||||||||||
Full Title: The effect of glucagon-like-peptide 1 (GLP-1) analogues on inflammation in humans with diabetic kidney disease. | |||||||||||||
Medical condition: Diabetic Kidney Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-002328-40 | Sponsor Protocol Number: HHSC/005 | Start Date*: 2007-05-18 | ||||||||||||||||
Sponsor Name:Imperial College London | ||||||||||||||||||
Full Title: A phase I safety and tolerability study of infusing the autologous progeny of an adult CD34+ subset into patients with type I diabetes mellitus and a successful renal transplant. | ||||||||||||||||||
Medical condition: Diabetes mellitus type 1 and succesful renal transplant | ||||||||||||||||||
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Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2012-002480-98 | Sponsor Protocol Number: MT-3995-E06 | Start Date*: 2012-10-26 | |||||||||||
Sponsor Name:Mitsubishi Tanabe Pharma Corporation (MTPC) | |||||||||||||
Full Title: A Randomised, Double-blind, Placebo-controlled Study to Evaluate the Effect on Urine Albumin-to-Creatinine Ratio (UACR), Pharmacodynamics, Safety, Tolerability and Pharmacokinetics of Multiple Oral... | |||||||||||||
Medical condition: Type II Diabetes Mellitus with Nephropathy and Albuminuria | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) LT (Completed) SK (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-005985-10 | Sponsor Protocol Number: PTF-REN-001 | Start Date*: 2008-03-03 | |||||||||||
Sponsor Name:Juan Francisco Navarro González | |||||||||||||
Full Title: Análisis del Efecto Renoprotector de la Pentoxifilina en Pacientes con Enfermedad Renal Crónica Secundaria a Nefropatía Diabética | |||||||||||||
Medical condition: Enfermedad renal crónica secundaria a nefropatía diabética. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-004523-19 | Sponsor Protocol Number: TIP0305 | Start Date*: 2008-02-08 | |||||||||||
Sponsor Name:Área de Trasplante y Terapia Celular - Hospital Central de Asturias | |||||||||||||
Full Title: Phase II clinical trial to evaluate the efficacy and safety in the use of pancreatic islets cells from cadaver donors for the treatment of Type-I Diabetes Mellitus in renal transplant patients. | |||||||||||||
Medical condition: Type-I Diabetes Mellitus in renal trasplant patients | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-003618-17 | Sponsor Protocol Number: ALT-711-0424 | Start Date*: 2008-05-07 | |||||||||||
Sponsor Name:JDRF Danielle Alberti Memorial Centre For Diabetes Complications Baker Heart Research Institute | |||||||||||||
Full Title: A Randomozed, Placebo-Controlled Trial of Alagebrium in Patients with Insulin-Dependent Type 1 Diabetes and Microalbuminuria | |||||||||||||
Medical condition: This is a double-blind phase 2 clinical study to evaluate the effects of alagebrium chloride (ALT-711) versus placebo on albumin excretion rate (as an early marker of diabetic nephropathy) in subje... | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-019206-16 | Sponsor Protocol Number: EBP-FHC-2010-3 | Start Date*: 2010-05-12 | |||||||||||
Sponsor Name:Medicinsk Forskning, Regionshospitalet Holstebro | |||||||||||||
Full Title: Effekten af atorvastatin på NO-systemet patienter med type 2 diabetes med nefropati | |||||||||||||
Medical condition: Diabetisk Nefropati Formålet er at måle effekten af atorvastatin på L-NMMA inducerede ændringer i den renale tubulære transport af natrium og vand , central hæmodynamik og vasoaktive hormoner hos... | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-011255-44 | Sponsor Protocol Number: 2009-278 | Start Date*: 2009-08-19 | |||||||||||
Sponsor Name:Steno Diabetes Center | |||||||||||||
Full Title: The effect of paricalcitol versus placebo on plasma NT-proBNP in patients with type 1 diabetes mellitus and diabetic nephropathy | |||||||||||||
Medical condition: Diabetes mellitus type 1 and diabetic nephropathy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-005954-62 | Sponsor Protocol Number: AIFA MICRO | Start Date*: 2007-01-25 | |||||||||||
Sponsor Name:IST. DI RICERCHE FARMACOLOG. M. NEGRI | |||||||||||||
Full Title: A prospective, randomized, open label blinded end point probe trial to evaluate whether, at comparable blood pressure control, combined therapy with the ACE inhibitor Benazepril and the angiotens... | |||||||||||||
Medical condition: Diabetic nephropathy | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-002491-40 | Sponsor Protocol Number: CLMB763X2202 | Start Date*: 2019-04-03 | |||||||||||
Sponsor Name:Novartis Pharma AG | |||||||||||||
Full Title: A randomized patient-and-physician blinded, placebo-controlled, 24-week study to assess the safety, tolerability and efficacy of LMB763 in patients with diabetic nephropathy | |||||||||||||
Medical condition: Diabetic Nephropathy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-001108-35 | Sponsor Protocol Number: NRA 6290010 | Start Date*: 2006-07-03 | |||||||||||
Sponsor Name:Clinic of University of Wuerzburg | |||||||||||||
Full Title: CHANGES OF LEFT VENTRICULAR MASS AND CARDIAC FUNCTION IN PATIENTS WITH ACTIVE ACROMEGALY DURING TREATMENT WITH THE GROWTH HORMONE RECEPTOR ANTAGONIST PEGVISOMANT: AN OPEN-LABELLED, PROSPECTIVE STUDY | |||||||||||||
Medical condition: Somavert (Pegvisomant) is approved for the treatment of acromegalic patients who have had an inadequate response to surgery and/or radiation therapy and/or other medical therapy as Somatostatin Ana... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
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