- Trials with a EudraCT protocol (576)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (6)
576 result(s) found for: Acute renal failure.
Displaying page 1 of 29.
EudraCT Number: 2008-002077-12 | Sponsor Protocol Number: MR-2008/001 | Start Date*: 2008-09-24 | |||||||||||||||||||||
Sponsor Name:AZIENDA OSPEDALIERA DI PERUGIA | |||||||||||||||||||||||
Full Title: Fenoldopam end Renal failure (FENO-HSR) | |||||||||||||||||||||||
Medical condition: Renal failure from ipoperfusion post Cardiac surgery | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-004361-12 | Sponsor Protocol Number: FER-CIT-2016-01 | Start Date*: 2017-03-27 | ||||||||||||||||
Sponsor Name:Fernando Sánchez | ||||||||||||||||||
Full Title: Oxidative stress and extracellular nucleosomes in critically ill patients with acute kidney failure treated with continuous renal replacement therapies. Effect of two anticoagulation strategies of ... | ||||||||||||||||||
Medical condition: Acute renal failure (ARF). | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Ongoing) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-007132-25 | Sponsor Protocol Number: AS-CD-04 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:EBI Anti Sepsis B.V. | |||||||||||||
Full Title: A randomized, double blind, parallel, placebo controlled, exploratory study to assess the effect of EA-230 on renal function and on safety and tolerability in patients at increased risk of developi... | |||||||||||||
Medical condition: acute renal failure | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-002109-32 | Sponsor Protocol Number: CORL2007 | Start Date*: 2007-05-10 | |||||||||||
Sponsor Name:AZIENDA SANITARIA OSPEDALIERA S. GIOVANNI BATTISTA DI TORINO | |||||||||||||
Full Title: USE OF FENOLDOPAM TO IMPROVE GLOMERULAR FILTRATION RATE IN EARLY RENAL DYSFUNCTION AFTER LIVER TRANSPLANTATION | |||||||||||||
Medical condition: Adult liver transplanted patients age > 18 years , with pre-transplantation normal renal function creatinine clearance 1ml/kg/min | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-018553-35 | Sponsor Protocol Number: SMF1482 | Start Date*: 2010-05-03 | |||||||||||
Sponsor Name:Gambro Lundia AB | |||||||||||||
Full Title: SMARTCIT - A NOVEL CITRATE BASED ANTICOAGULATION | |||||||||||||
Medical condition: Acute renal failure | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-004426-24 | Sponsor Protocol Number: 951/07 | Start Date*: 2007-07-06 | |||||||||||
Sponsor Name:POLICLINICO UNIVERSITARIO AGOSTINO GEMELLI | |||||||||||||
Full Title: PROSTACYCLIJN VERSUS HEPARIN AS ANTICOAGULANT IN CONTINUOUS VENO-VENOUS HEMODIAFILTRATION | |||||||||||||
Medical condition: Acute renale failure in intensive unit | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-014562-26 | Sponsor Protocol Number: CERL080AES08 | Start Date*: 2010-02-17 | ||||||||||||||||
Sponsor Name:Novartis Farmacéuitica S.A | ||||||||||||||||||
Full Title: Estudio multicéntrico, aleatorizado, abierto de maximización de micofenolato sódico (MFS) versus micofenolato mofetilo (MMF) para minimizar la dosis de tacrolimus en pacientes trasplantados renale... | ||||||||||||||||||
Medical condition: Profilaxis del rechazo agudo en trasplante alogénico renal. Minimizar la dosis de tacrolimus en pacientes trasplantados renales en mantenimiento | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2006-001407-11 | Sponsor Protocol Number: Certican MHH PRTx01 | Start Date*: 2006-07-18 | |||||||||||
Sponsor Name:Medizinische Hochschule Hannover | |||||||||||||
Full Title: A single center study investigating ciclosporine A microemulsion in combination with basiliximab and prednisolon and switch to low-dose ciclosporine A and everolimus without steroids in the prevent... | |||||||||||||
Medical condition: Kidney transplantation after end stage renal failure | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-006014-20 | Sponsor Protocol Number: FARM6X822T | Start Date*: 2009-01-19 | |||||||||||
Sponsor Name:CONSORZIO MARIO NEGRI SUD | |||||||||||||
Full Title: Effects of the dose of erythropoiesis stimulating agents on cardiac-cerebrovascular outcomes and quality of life in hemodialysis patients. The DOSe of Erythropoietins (DOSE) trial. | |||||||||||||
Medical condition: End stage kidney disease and anemia, treated with hemodialysis for renal replacement therapy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-016801-40 | Sponsor Protocol Number: IP-001-09 | Start Date*: 2016-01-26 | |||||||||||
Sponsor Name:IPERBOREAL PHARMA | |||||||||||||
Full Title: Efficacy and Safety assessments of a peritoneal dialysis solution containing Glucose, Xylitol and L-Carnitine compared to standard PD solutions in Continuous Ambulatory Peritoneal Dialysis (CAPD) | |||||||||||||
Medical condition: Patients with ESRD treated by CAPD | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-003866-16 | Sponsor Protocol Number: AP REN 01-01 | Start Date*: 2009-03-03 | ||||||||||||||||
Sponsor Name:AM-Pharma B.V. | ||||||||||||||||||
Full Title: A Phase-II, double-blind, randomized, placebo-controlled proof of concept study on the safety and early efficacy of Alkaline Phosphatase in sepsis patients with Renal Failure. | ||||||||||||||||||
Medical condition: Sepsis with Renal Failure | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: BE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2004-000304-41 | Sponsor Protocol Number: FG-506E-12-03 | Start Date*: 2004-12-15 | |||||||||||
Sponsor Name:Astellas Pharma GmbH | |||||||||||||
Full Title: A MULTICENTRE, 1:1 RANDOMISED, DOUBLE BLIND, TWO ARM PARALLEL GROUP STUDY TO EVALUATE AND COMPARE THE EFFICACY AND SAFETY OF MODIFIED RELEASE TACROLIMUS FK506E (MR4) VERSUS TACROLIMUS FK506 IN COMB... | |||||||||||||
Medical condition: Patients with end stage kidney disease who will undergo renal transplantation | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) SE (Completed) HU (Completed) FI (Completed) AT (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-022584-35 | Sponsor Protocol Number: TUD-BRIDGE-046 | Start Date*: 2011-11-25 | |||||||||||
Sponsor Name:Dresden Universtity of Technology | |||||||||||||
Full Title: Clofarabine salvage therapy in patients with relapsed or refractory AML The BRIDGE Trial | |||||||||||||
Medical condition: Patients with AML >40 years of age with untreated relapse or refractory disease after a minimum of one standard induction therapy. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-000644-16 | Sponsor Protocol Number: Dor1.0 | Start Date*: 2011-05-03 | |||||||||||||||||||||
Sponsor Name:University of Tartu, Clinic of Anaesthesiology and Intensive Care | |||||||||||||||||||||||
Full Title: High volume haemodiafiltration in treatment of severe sepsis -- impact on pharmacokinetics of doripenem and piperacillin tazobactam and inflammatory response | |||||||||||||||||||||||
Medical condition: adult intensive care patient with severe sepsis or septic shock and acute renal failure requiring renal replacement therapy | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: EE (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2004-000520-32 | Sponsor Protocol Number: FG-506-02-42 | Start Date*: 2005-01-26 | |||||||||||
Sponsor Name:Fujisawa GmbH | |||||||||||||
Full Title: A MULTICENTRE, RANDOMISED, OPEN CLINICAL STUDY TO COMPARE THE EFFICACY AND SAFETY OF A COMBINATION OF TACROLIMUS AND MYCOPHENOLATE MOFETIL BASED REGIMEN WITH OR WITHOUT INDUCTION IN ELDERLY RECIPIE... | |||||||||||||
Medical condition: Patients with end stage kidney disease who will undergo primary renal transplantion or retransplantation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-006515-28 | Sponsor Protocol Number: ASST_FARM_2021TMO_FT14 | Start Date*: 2022-06-07 | |||||||||||
Sponsor Name:AZIENDA SOCIO SANITARIA TERRITORIALE DEGLI SPEDALI CIVILI DI BRESCIA | |||||||||||||
Full Title: Prospective Phase II study on Safety and Efficacy of Fludarabine plus Treosulfan (14g) (FT14) conditioning regimen for allogeneic Stem Cell Transplantation (allo-SCT) in Acute Myeloid Leukemia (AML... | |||||||||||||
Medical condition: Acute Myeloid Leukemia (AML) patients (=40 <65years) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-015114-22 | Sponsor Protocol Number: ML22916 | Start Date*: 2010-08-10 | |||||||||||
Sponsor Name:Roche Pharma AG | |||||||||||||
Full Title: A randomized controlled, single-blind, proof- of- concept-study to investigate the protective effects of early treatment with C.E.R.A. in patients with chronic kidney disease on renal disease progr... | |||||||||||||
Medical condition: diabetic and transplanted CKD stage III patients | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-004152-10 | Sponsor Protocol Number: EMPATHY | Start Date*: 2020-01-30 | ||||||||||||||||
Sponsor Name:IRCCS- ISTITUTO DI RICERCHE FARMACOLOGICHE MARIO NEGRI | ||||||||||||||||||
Full Title: Evaluating the Short-Term Renal and Systemic Effects of SGLT2 Inhibition in Non-Diabetic Patients at Risk of Accelerated GFR Decline Because of Glomerular Hyperfiltration: a sequential OFF-ON-OFF S... | ||||||||||||||||||
Medical condition: Obesity Renal chronic disease | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-003968-22 | Sponsor Protocol Number: ETFLCHD01 | Start Date*: 2008-02-04 | ||||||||||||||||||||||||||
Sponsor Name:University Hospital Birmingham | ||||||||||||||||||||||||||||
Full Title: European Trial of Free Light Chain Removal by Extended Haemodialysis in Cast Nephropathy | ||||||||||||||||||||||||||||
Medical condition: Multiple myeloma patients with acute dialysis dependent renal failure resulting from cast nephropathy. | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: GB (Completed) DE (Completed) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-004888-41 | Sponsor Protocol Number: IPeRStudy | Start Date*: 2012-12-28 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA DI BOLOGNA POLICLINICO S. ORSOLA M. MALPIGHI | |||||||||||||
Full Title: Intensive Phosphate Control in Development of Renal End Points and Mortality in CKD (the IPeR Study) | |||||||||||||
Medical condition: Patients with Chronic Kidney Disease (CKD) not yet on dialysis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
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