- Trials with a EudraCT protocol (86)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (18)
86 result(s) found for: Chronic renal insufficiency.
Displaying page 1 of 5.
EudraCT Number: 2005-003233-41 | Sponsor Protocol Number: SVCARB00105 | Start Date*: 2005-10-25 | |||||||||||
Sponsor Name:Genzyme Europe BV | |||||||||||||
Full Title: An open label, dose titration study of sevelamer carbonate tablets dosed three times a day in hyperphosphatemic chronic kidney disease patients not on dialysis | |||||||||||||
Medical condition: Chronic kidney disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) DE (Completed) DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-004835-26 | Sponsor Protocol Number: D169AL00005 | Start Date*: 2021-05-24 | |||||||||||
Sponsor Name:IRCCS-A.O.U. SAN MARTINO-IST | |||||||||||||
Full Title: Single-center, randomized, controlled study to evaluate the effects of a six-month treatment with renal glucose transport inhibitor (SGLT2i) drugs on markers of senescence, inflammation and tubuloi... | |||||||||||||
Medical condition: Chronic Kidney Deseas | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-004496-22 | Sponsor Protocol Number: 13273 | Start Date*: 2008-11-13 | |||||||||||
Sponsor Name:Bayer Health Care AG | |||||||||||||
Full Title: Prospective non-randomized (pharmacoepidemiologic) cohort study (open-label, multicenter) to assess the magnitude of potential risk with the administration of Gadovist® in patients with moderate to... | |||||||||||||
Medical condition: Patients with moderate to severe renal impairment. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) AT (Completed) FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-001682-33 | Sponsor Protocol Number: 6176/RADS2 | Start Date*: 2012-09-06 | |||||||||||||||||||||
Sponsor Name:Newcastle upon Tyne Hospitals NHS Foundation Trust | |||||||||||||||||||||||
Full Title: Combined Immunotherapy and Trophic Adrenocortical Stimulation in New Onset Autoimmune Addison’s Disease | |||||||||||||||||||||||
Medical condition: Autoimmune Addison's disease: autoimmune primary adrenal insufficiency | |||||||||||||||||||||||
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Population Age: Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: GB (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2020-003229-47 | Sponsor Protocol Number: KEEP-ON | Start Date*: 2022-01-12 | |||||||||||||||||||||
Sponsor Name:Instituto de Investigación Sanitaria INCLIVA | |||||||||||||||||||||||
Full Title: Phase III, multicenter, open-label, randomized clinical trial to evaluate efficacy of Sodium Zirconium Cyclosilicate (Lokelma) compared to standard of care to manage hyperkalemia in patients with c... | |||||||||||||||||||||||
Medical condition: Hyperkalemia in patients with chronic kidney disease (CKD) and heart failure history | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-002856-18 | Sponsor Protocol Number: RB12.079 | Start Date*: 2013-03-22 | ||||||||||||||||
Sponsor Name:CHRU de Brest | ||||||||||||||||||
Full Title: ALdosterone antagonist Chronic HEModialysis Interventional Survival Trial | ||||||||||||||||||
Medical condition: | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: FR (Ongoing) BE (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-002407-17 | Sponsor Protocol Number: DN 2 | Start Date*: Information not available in EudraCT |
Sponsor Name:Technical University Dresden | ||
Full Title: Effects of rosiglitazone on renal hemodynamics and proteinuria of type 2 diabetic patients with renal insufficiency due to overt diabetic nephropathy | ||
Medical condition: type 2 diabetic patients with proteinuria and chronic renal failure due to overt diabetic nephropathy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2015-005003-88 | Sponsor Protocol Number: SIM15 | Start Date*: 2016-03-15 | |||||||||||
Sponsor Name:Cambridge University Hospitals NHS Foundation Trust and University of Cambridge | |||||||||||||
Full Title: Survival Improvement with Cholecalciferol in Patients on Dialysis – The SIMPLIFIED Registry Trial | |||||||||||||
Medical condition: Kidney Failure (requiring dialysis). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-000726-10 | Sponsor Protocol Number: ADAPT | Start Date*: 2021-06-23 | |||||||||||
Sponsor Name:IRCCS- ISTITUTO DI RICERCHE FARMACOLOGICHE MARIO NEGRI | |||||||||||||
Full Title: Evaluating the short-term renal and systemic effects of Dapagliflozin in non-diabetic patients with stage IV CKD at risk of ESKD because of severe renal insufficiency and persistent proteinuria: A ... | |||||||||||||
Medical condition: Non-diabetic stage IV Chronic Kidney Disease (CKD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-002221-31 | Sponsor Protocol Number: CCB-CRC-05-1 | Start Date*: 2005-08-11 |
Sponsor Name:Clinic for Nephrology | ||
Full Title: Efficacy of niacin on phosphatic metabolism in patients with renal insufficiency | ||
Medical condition: Exam the efficacy of niaspan in phosphate metabolism of patients with renal insufficiency, different exam for dialysis and predialysis patients | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2021-006487-24 | Sponsor Protocol Number: ADNorGC | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Helse Bergen HF | |||||||||||||
Full Title: A registry-based, open-label, randomized study to investigate quality-of-life with Plenadren compared with Cortison in participants aged 16-80 with newly diagnosed primary adrenal insufficiency | |||||||||||||
Medical condition: Primary adrenal insufficiency | |||||||||||||
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Population Age: Adolescents, Under 18, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NO (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-001899-32 | Sponsor Protocol Number: RESINFENOL | Start Date*: 2017-08-17 |
Sponsor Name:Dr. Abelardo Aguilera Peralta | ||
Full Title: Crossover and randomized clinical trial on the effect of Resincolestiramine in the intestinal absorption of new uremic toxins in patients in hemodialysis with chronic renal insufficiency | ||
Medical condition: Chronic renal insufficiency | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2013-002522-23 | Sponsor Protocol Number: BAY1067197/16782 | Start Date*: 2013-12-20 | |||||||||||
Sponsor Name:Bayer Healthcare AG | |||||||||||||
Full Title: A double blinded, placebo controlled, study to investigate the safety, tolerability, pharmacokinetics and acute cardiovascular responses of a 7 day oral treatment with the partial adenosine A1 rece... | |||||||||||||
Medical condition: Chronic systolic heart failure | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) IT (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-002160-22 | Sponsor Protocol Number: 0431-028 | Start Date*: 2004-11-17 | |||||||||||
Sponsor Name:Merck & Co., Inc. | |||||||||||||
Full Title: A Multicenter, Randomized, Double-Blind Study to Evaluate the Safety of MK-0431 Monotherapy in Patients With Type 2 Diabetes Mellitus and Chronic Renal Insufficiency Who Have Inadequate Glycemic Co... | |||||||||||||
Medical condition: Type 2 Diabetes Mellitus Chronic Renal Insufficiency [MedDRA classification code: 10050441] | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-000622-22 | Sponsor Protocol Number: ASAP | Start Date*: 2012-07-20 | |||||||||||
Sponsor Name:Fundació Clínic per a la Recerca Biomèdica | |||||||||||||
Full Title: Aspirin for the enhancement of trophoblastic invasion in women with abnormal uterine artery Doppler at 11-14 weeks of gestation | |||||||||||||
Medical condition: Placental insufficiency | |||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-001906-26 | Sponsor Protocol Number: 2007-22-INJ-17 | Start Date*: 2008-09-10 | |||||||||||
Sponsor Name:HEXAL AG | |||||||||||||
Full Title: Randomized, controlled, double-blind multicenter safety study to evaluate the safety and immunogenicity of subcutaneous EPO HEXAL vs. ERYPO® in the treatment of anemia associated with chronic renal... | |||||||||||||
Medical condition: anemia associated with chronic renal insufficiency in predialysis patients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) AT (Prematurely Ended) SK (Completed) FR (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-002208-17 | Sponsor Protocol Number: DNB-001-CT002 | Start Date*: 2007-08-14 | ||||||||||||||||
Sponsor Name:Danube Pharmaceuticals | ||||||||||||||||||
Full Title: A Phase IIa, Multi-Center, Double Blind, Randomized, Placebo-Controlled Trial to Evaluate the Efficacy, Safety and Pharmacokinetics of DNB-001 in Patients with Angina Pectoris and Moderate Chronic ... | ||||||||||||||||||
Medical condition: Angina pectoris and renal insufficiency whilst undergoing percutaneous coronary intervention (PCI). | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-021263-33 | Sponsor Protocol Number: 3001101 | Start Date*: 2011-05-24 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Sykehuset i Vestfold HF | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: PERIOPERATIVE LEVOSIMENDAN INFUSION IN PATIENTS WITH HEART FAILURE UNDERGOING NON-CARDIAC SURGERY: A PROSPECTIVE, RANDOMISED, PLACEBO-CONTROLLED, DOUBLE-BLIND, MULTICENTER STUDY | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Patients with serious cardiac failure scheduled for non-cardiac surgery | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: SE (Prematurely Ended) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-003719-37 | Sponsor Protocol Number: GN15CA580 | Start Date*: 2017-07-25 | ||||||||||||||||
Sponsor Name:NHS Greater Glasgow and Clyde [...] | ||||||||||||||||||
Full Title: StUdies of empaGliflozin and its cArdiovascular, Renal and metabolic effects in patients with Diabetes Mellitus (or prediabetes) and Heart Failure (SUGAR-DM-HF) | ||||||||||||||||||
Medical condition: Chronic heart failure with left ventricular systolic dysfunction | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-003968-39 | Sponsor Protocol Number: 2015CA02 | Start Date*: 2017-09-19 | ||||||||||||||||||||||||||
Sponsor Name:University of Dundee/NHS Tayside | ||||||||||||||||||||||||||||
Full Title: Renal and Cardiovascular Effects of SGLT2 inhibition in combination with loop diuretics in diabetic patients with chronic heart failure. | ||||||||||||||||||||||||||||
Medical condition: Type 2 diabetes and heart failure | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||||||||||||
Trial results: View results |
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