- Trials with a EudraCT protocol (40)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (3)
40 result(s) found for: Eplerenone.
Displaying page 2 of 2.
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EudraCT Number: 2015-002519-14 | Sponsor Protocol Number: 2015-775 | Start Date*: 2015-08-25 | |||||||||||
Sponsor Name:Herlev Hospital | |||||||||||||
Full Title: The MIRAD study - Mineralocorticoid Receptor Antagonists in Type 2 Diabetes. A randomised, double-blind, placebo-controlled study of the effect of Mineralocorticoid Receptor Antagonists in Type 2 D... | |||||||||||||
Medical condition: diabetes (type 2) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-002518-35 | Sponsor Protocol Number: 2011-402 | Start Date*: 2012-02-22 | |||||||||||
Sponsor Name:Karl Emil Kristensen | |||||||||||||
Full Title: The effect of aldosterone on the development of chronic allograft nephropathy after kidney transplantation | |||||||||||||
Medical condition: Chronic allograft nephropathy in kidney transplants, defined as tubular atrophy and interstitial fibrosis in graft biopsy (Banff criteria) | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-003351-12 | Sponsor Protocol Number: A6141079 | Start Date*: 2005-10-27 | |||||||||||
Sponsor Name:Pfizer Ltd | |||||||||||||
Full Title: The effect of eplerenone versus placebo on cardiovascular mortality and heart failure hospitalization in subjects with NYHA Class II Chronic Systolic Heart Failure | |||||||||||||
Medical condition: Chronic systolic heart failure | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) IE (Completed) SK (Completed) SE (Completed) GB (Completed) ES (Completed) HU (Completed) BE (Completed) PT (Completed) GR (Completed) IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-019844-38 | Sponsor Protocol Number: A6141116 | Start Date*: 2010-08-12 | |||||||||||
Sponsor Name:Pfizer, S.A | |||||||||||||
Full Title: A double-blind, randomized, placebo-controlled trial evaluating the safety and efficacy of early the treatment with Eplerenone in patients with acute myocardial infarction. Estudio doble ciego, al... | |||||||||||||
Medical condition: Infarto agudo de miocardio | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) SK (Completed) CZ (Completed) HU (Completed) GB (Completed) DE (Completed) NL (Completed) GR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-001327-41 | Sponsor Protocol Number: IMIB-RMV-2021-02 | Start Date*: 2021-07-12 |
Sponsor Name:Fundación para la formación e investigación sanitarias de la Región de Murcia | ||
Full Title: Withdrawal of pharmacological treatment in patients responding to cardiac resynchronization therapy: Open and randomized study | ||
Medical condition: Heart failure | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2017-003555-35 | Sponsor Protocol Number: PAT-DEU-402 | Start Date*: 2017-11-17 | |||||||||||
Sponsor Name:Fresenius Medical Care Nephrologica Deutschland GmbH | |||||||||||||
Full Title: A Multicentre, Randomised, Open-label, Parallel-Group Pilot Study to Evaluate the Efficacy of Patiromer in Optimising Mineralocorticoid Receptor Antagonist Therapy in Heart Failure Subjects with Hy... | |||||||||||||
Medical condition: Heart Failure with reduced ejection fraction (HFrEF) subjects with hyperkalaemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-011291-29 | Sponsor Protocol Number: RACE 3 | Start Date*: 2011-08-16 | |||||||||||
Sponsor Name:Interuniversity Cardiology Institute of the Netherlands (ICIN) | |||||||||||||
Full Title: Routine versus Aggressive Upstream Rhythm Control for Prevention of Early Atrial Fibrillation in Heart Failure: RACE 3 | |||||||||||||
Medical condition: atrial fibrillation | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) NL (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-000773-23 | Sponsor Protocol Number: I4M-MC-MRAC | Start Date*: 2012-04-23 | |||||||||||
Sponsor Name:Eli Lilly and Company | |||||||||||||
Full Title: Study of the Safety and Efficacy of LY2623091 in Chronic Kidney Disease Patients | |||||||||||||
Medical condition: Chronic kidney disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BG (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-003139-19 | Sponsor Protocol Number: CLCI699A2201 | Start Date*: 2008-09-12 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A multi-center, randomized, double-blind, placebo and active controlled, parallel group, dose finding study to evaluate the efficacy and safety of LCI699 compared to placebo after 8 weeks treatment... | |||||||||||||
Medical condition: Essential Hypertension | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) SE (Completed) NL (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-001192-29 | Sponsor Protocol Number: cv-08/025 | Start Date*: 2008-06-03 |
Sponsor Name:Fundación Investigación y Desarrollo en el Area Cardiovascular | ||
Full Title: “Evaluación mediante proteómica de biomarcadores proteicos asociados con el tratamiento con Eplerenona versus espironolactona en pacientes post-infarto agudo de miocardio, diabéticos con hipertensi... | ||
Medical condition: Disfunción ventricular leve-moderada post-infarto agudo de miocardio en pacientes diabéticos con hipertensión arterial no controlada. Low-moderate ventricular dysfunction in post-acute coronary sy... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2008-007338-23 | Sponsor Protocol Number: CLCI699A2216 | Start Date*: 2009-02-18 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A phase II, randomized, double-blind, placebo and active controlled, parallel group, multi-center, dose ranging study to evaluate the efficacy and safety of LCI699 compared to placebo after 8 weeks... | |||||||||||||
Medical condition: resistant hypertension | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IS (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-012445-35 | Sponsor Protocol Number: ALBLOCK-2 | Start Date*: 2009-11-26 | |||||||||||
Sponsor Name:Herlev Hospital | |||||||||||||
Full Title: Aldosterone receptor blockade in patients with chronic kidney disease. Influence on arterial stiffness and kidney function. | |||||||||||||
Medical condition: Chronic kidney disease, stages 3 and 4. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-001264-22 | Sponsor Protocol Number: SILK/Eplerenone1 | Start Date*: 2012-11-08 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Region Skåne | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: Eplerenone and spironolactone in male patients with ascites due to liver cirrhosis. A Swedish prospective randomized multicenter study of efficacy and endocrinologic side effects. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Ascites complicating liver cirrhosis in males | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Elderly | Gender: Male | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: SE (Ongoing) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-005176-35 | Sponsor Protocol Number: ESR-19-20262 | Start Date*: 2021-01-14 |
Sponsor Name:Sahlgrenska University Hospital | ||
Full Title: OPtimizing Aldosterone Receptor Antagonist Therapy by Sodium Zirconium Cyclosili-cate in Heart Failure (OPRA-HF) | ||
Medical condition: Heart failure | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2011-000414-20 | Sponsor Protocol Number: CHANCE-HF | Start Date*: 2011-08-02 | |||||||||||
Sponsor Name:Consorcio de Apoyo a la Investigacion Biomedica en Red (CAIBER) | |||||||||||||
Full Title: Ensayo aleatorizado controlado sobre la terapia guiada por el antígeno carbohidrato 125 en los pacientes dados de alta por insuficiencia cardiaca aguda: efecto sobre la mortalidad a 1 año. | |||||||||||||
Medical condition: acute heart failure | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-002605-53 | Sponsor Protocol Number: EVEDES | Start Date*: 2008-05-20 | ||||||||||||||||
Sponsor Name:Fundació Institut de Recerca de l'Hospital de la Santa Creu i de Sant Pau | ||||||||||||||||||
Full Title: Antagonistas aldosterónicos en el tratamiento de pacientes con ventrículo derecho sistémico: ensayo clínico aleatorizado. | ||||||||||||||||||
Medical condition: Transposición de grandes vasos tratada mediante la técnica de redirección auricular (técnicas de Senning o Mustard). | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: ES (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-005351-27 | Sponsor Protocol Number: 2015CD007B | Start Date*: 2016-02-17 | ||||||||||||||||
Sponsor Name:Royal Brompton & Harefield NHS Foundation Trust | ||||||||||||||||||
Full Title: A randomised controlled pilot trial of the feasibility and safety of therapy withdrawal in asymptomatic patients with a prior diagnosis of dilated cardiomyopathy & recovered cardiac function. | ||||||||||||||||||
Medical condition: Dilated Cardiomyopathy with recovered cardiac function | ||||||||||||||||||
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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: 2020-003312-27 | Sponsor Protocol Number: D9480C00018 | Start Date*: 2021-03-02 | |||||||||||
Sponsor Name:AstraZeneca AB | |||||||||||||
Full Title: Phase IV, Double-Blind, Placebo-Controlled, Randomized-Withdrawal Trial Evaluating Sodium Zirconium Cyclosilicate (SZC) for the Management of Hyperkalaemia in Patients with Symptomatic Heart Failur... | |||||||||||||
Medical condition: Hyperkalemia in Patients with Symptomatic Heart Failure. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) ES (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-000490-40 | Sponsor Protocol Number: S320.2.003 | Start Date*: 2007-06-20 | |||||||||||
Sponsor Name:Solvay Pharmaceuticals GmbH | |||||||||||||
Full Title: Randomised, Double-Blind, Placebo-Controlled, Multi-Center, Sequential Cohort Study to Evaluate the Effect of SLV320 in Addition to Chronic Furosemide Treatment on Renal Function in Subjects with C... | |||||||||||||
Medical condition: Renal Function in Subjects with Congestive Heart Failure and Impaired Renal Function who are on Chronic Furosemide Treatment | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) CZ (Prematurely Ended) ES (Ongoing) DE (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-005030-38 | Sponsor Protocol Number: PAT-CR-302 | Start Date*: 2019-08-10 | |||||||||||
Sponsor Name:Vifor Pharma, Inc. | |||||||||||||
Full Title: A Multicenter, Double-blind, Placebo-controlled, Randomized Withdrawal, Parallel Group Study of Patiromer for the Management of Hyperkalemia in Subjects Receiving Renin-Angiotensin-Aldosterone Syst... | |||||||||||||
Medical condition: Management of hyperkalemia due to renin-angiotension-aldosterone system medications in patients treated for heart failure. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Completed) CZ (Completed) NL (Completed) ES (Ongoing) HU (Completed) DE (Completed) BG (Completed) GB (GB - no longer in EU/EEA) BE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
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