- Trials with a EudraCT protocol (3,812)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
3,812 result(s) found for: Failure Rate.
Displaying page 1 of 191.
EudraCT Number: 2012-001134-33 | Sponsor Protocol Number: iCHF | Start Date*: 2012-11-21 | |||||||||||
Sponsor Name:Universitätsklinikum Ulm | |||||||||||||
Full Title: Randomized, Double-Blind, Placebo-Controlled Trial of Ferric Carboxymaltose Versus Placebo in Patients with Congestive Heart Failure | |||||||||||||
Medical condition: Congestive heart failure (CHF) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-020657-14 | Sponsor Protocol Number: ALF-5755_P2_ALF | Start Date*: 2011-07-04 | |||||||||||
Sponsor Name:Alfact Innovation | |||||||||||||
Full Title: A multicentre, double-blind, randomized, placebo-controlled study to evaluate the efficacy and the safety of ALF-5755 in patients with nonacetaminophen severe acute hepatitis and early stage acute ... | |||||||||||||
Medical condition: Acute liver failure | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-006237-27 | Sponsor Protocol Number: CT/P004/HF/08/02_01 | Start Date*: 2009-10-12 | |||||||||||
Sponsor Name:Torrent Pharmaceuticals Ltd. | |||||||||||||
Full Title: Safety and efficacy of TRC4186 in the treatment of stable heart failure associated with HbA1c >= 6 % or type 2 diabetes receiving oral hypoglycaemic therapy (with or without additional insulin) as ... | |||||||||||||
Medical condition: heart failure associated with impaired glucose tolerance or type 2 diabetes | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-001971-30 | Sponsor Protocol Number: CLCZ696B2317 | Start Date*: 2014-11-22 | |||||||||||
Sponsor Name:Novartis Pharma services AG | |||||||||||||
Full Title: A multicenter study to evaluate safety and tolerability in patients with chronic heart failure and reduced ejection fraction from PARADIGM-HF receiving open label LCZ696 | |||||||||||||
Medical condition: Heart failure with reduced ejection fraction | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LV (Completed) LT (Completed) FI (Completed) NL (Completed) CZ (Completed) SE (Completed) SK (Completed) HU (Completed) PT (Completed) DK (Completed) EE (Completed) ES (Completed) IT (Completed) DE (Completed) BE (Completed) BG (Completed) FR (Completed) PL (Completed) | |||||||||||||
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: 2007-006660-30 | Sponsor Protocol Number: RO730 | Start Date*: 2009-03-11 | |||||||||||
Sponsor Name:Hull and East Yorkshire Hospitals NHS Trust | |||||||||||||
Full Title: Contemporary Heart Failure Management : A Randomised, Placebo-Controlled Trial to Measure the Effects of Low Dose Digoxin on Haemodynamics and Symptoms in Patients with Heart Failure | |||||||||||||
Medical condition: Heart Failure | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-002450-37 | Sponsor Protocol Number: IOEX2017 | Start Date*: 2018-12-11 | ||||||||||||||||
Sponsor Name:AZIENDA OSPEDALIERO-UNIVERSITARIA CAREGGI | ||||||||||||||||||
Full Title: Renal function evaluation through iohexol method in the elderly with sarcopenia and low serum creatinine | ||||||||||||||||||
Medical condition: Elderly sarcopenia patients with low serum creatinine and suspected chronic kidney disease | ||||||||||||||||||
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Population Age: Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-001287-34 | Sponsor Protocol Number: BAY1067197/16718 | Start Date*: 2013-11-04 | |||||||||||
Sponsor Name:Bayer HealthCare AG | |||||||||||||
Full Title: A single blind, placebo controlled pilot study to explore the safety and tolerability of a single oral dose of 30 mg BAY 1067197 in patients with chronic heart failure on the background of preexist... | |||||||||||||
Medical condition: Heart failure | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-000410-37 | Sponsor Protocol Number: 310107 | Start Date*: 2007-09-26 | |||||||||||
Sponsor Name:University Of Tuebingen | |||||||||||||
Full Title: Determination of glomerular filtration rate (GFR) using MR nephrography in patients with chronic kidney disease. | |||||||||||||
Medical condition: Chronic kidney disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-004600-53 | Sponsor Protocol Number: RBK03-16-00389 | Start Date*: 2018-06-08 | ||||||||||||||||||||||||||
Sponsor Name:WÖRWAG Pharma GmbH & Co. KG | ||||||||||||||||||||||||||||
Full Title: MACH 2 - Magnesium orotate in severe congestive heart failure - Part 2 | ||||||||||||||||||||||||||||
Medical condition: Heart failure with reduced ejection fraction | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
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: 2019-004186-40 | Sponsor Protocol Number: CV019-010 | Start Date*: 2020-06-18 | |||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
Full Title: A Randomized, Double-Blinded, Placebo-Controlled, Study to Evaluate the Safety and Tolerability of BMS-986259 in Stabilized Patients Hospitalized for Acute Decompensated Heart Failure | |||||||||||||
Medical condition: Heart failure | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) NL (Completed) GR (Completed) PL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-003496-29 | Sponsor Protocol Number: I13034 | Start Date*: 2014-10-24 | |||||||||||
Sponsor Name:University Hospital, Limoges | |||||||||||||
Full Title: Designing a Bayesian model of the plasma clearance of Calcium edetate de sodium, with a limited sampling strategy for the calculation of Glomerular Filtration Rate (GFR) and validity assessment com... | |||||||||||||
Medical condition: Chronic Kidney Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-001200-23 | Sponsor Protocol Number: CCFM 103/208 | Start Date*: 2008-07-13 | |||||||||||
Sponsor Name:FONDAZIONE MONZINO CENTRO CARDIOLOGICO | |||||||||||||
Full Title: A Study to Evaluate the Effectiveness of Induced Diuresis with Matched Hydration Therapy Compared to Standard Overnight Hydration in the Prevention of Contrast Induced Nephropathy | |||||||||||||
Medical condition: Patients with moderate to severe renal failure candidates to angiographic procedures at high risk for CIN | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-005607-92 | Sponsor Protocol Number: QUIDHF_v3.0_20161130 | Start Date*: 2016-08-04 | |||||||||||
Sponsor Name:QUANTUM GENOMICS | |||||||||||||
Full Title: A Phase II randomized, placebo controlled, double-blind, multi-centre study to assess safety and efficacy of incremental doses of QGC001 in patients upon discharge or following hospitalization for ... | |||||||||||||
Medical condition: Patient with worsening chronic heart failure with left ventricular systolic dysfunction | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Prematurely Ended) NO (Ongoing) GB (Prematurely Ended) PL (Prematurely Ended) HU (Ongoing) CZ (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-001994-27 | Sponsor Protocol Number: 2006B180 | Start Date*: 2007-09-03 | |||||||||||
Sponsor Name:Netherlands Heart Foundation | |||||||||||||
Full Title: The effect of beta-adrenergic receptor blockade on sympathetic activity and coagulation in patients with heart failure (BACH-F study) | |||||||||||||
Medical condition: Congestive heart failure | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
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: 2005-005658-37 | Sponsor Protocol Number: 2006-1 | Start Date*: 2006-07-07 | |||||||||||
Sponsor Name:Dpt. of Urology -K. Aarhus University Hospital | |||||||||||||
Full Title: A randomized, multi-center study to assess the effect of Darbepoetin alfa (Aranesp®) for the treatment of anemia in patients with advanced hormone independent prostate cancer and anaemia | |||||||||||||
Medical condition: In an open randomised, multi-center study to identify the haematopoietic response to Aranesp® (Darbepoetin 6,75 mcg/kg) administrated every fourth week compared to standard care of treatment in pat... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: DK (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-000948-98 | Sponsor Protocol Number: H-3-2011-154 | Start Date*: 2012-05-03 | |||||||||||
Sponsor Name:Rigshospitalet | |||||||||||||
Full Title: Effect of epinephrine on systemic absorption of mepivacaine administered for brachial plexus block in patients with end-stage renal disease | |||||||||||||
Medical condition: End-stage renal disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-016531-35 | Sponsor Protocol Number: SPD405-703 | Start Date*: 2010-05-18 | |||||||||||
Sponsor Name:Shire Pharmaceutical Development Ltd | |||||||||||||
Full Title: A Proof of Concept, Phase 2a, Double-blind, Parallel Group, Randomised, Placebo controlled Study to Assess the Effect of Lanthanum Carbonate on intact FGF23 in Normo-phosphataemic Subjects with Sta... | |||||||||||||
Medical condition: Chronic Kidney Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
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