- Trials with a EudraCT protocol (88)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
88 result(s) found for: Chronic Heart Failure (CHF).
Displaying page 1 of 5.
EudraCT Number: 2005-004487-22 | Sponsor Protocol Number: BMI 001 / SMR-1389 | Start Date*: 2005-11-25 | |||||||||||
Sponsor Name:Bio-Medisinsk Innovasjon AS | |||||||||||||
Full Title: A Proof of Biological Efficacy Study Assessing the Potential of Piboserod a Specific 5-HT4 Antagonist for the Treatment of Symptomatic Congestive Heart Failure in stable outpatients NYHA class II-I... | |||||||||||||
Medical condition: Congestive heart failure | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) GB (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-002809-48 | Sponsor Protocol Number: CRO782 | Start Date*: 2013-04-17 | |||||||||||
Sponsor Name:Imperial College London and Imperial College Healthcare NHS Trust | |||||||||||||
Full Title: Investigation of the safety and feasibility of AAV1/SERCA2a gene transfer in patients with chronic heart failure and a left ventricular assist device | |||||||||||||
Medical condition: Advanced heart failure | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-000220-33 | Sponsor Protocol Number: CLCZ696BDE03 | Start Date*: 2019-02-04 | |||||||||||
Sponsor Name:Novartis Pharma GmbH | |||||||||||||
Full Title: A randomized, double-blind, active-controlled study to assess the effect of sacubitril/valsartan compared with enalapril to improve erectile function in patients with heart failure with reduced eje... | |||||||||||||
Medical condition: Patients with heart failure with reduced ejection fraction (HFrEF) and erectile dysfunction (ED) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
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: 2015-002673-38 | Sponsor Protocol Number: CRLX030A2211 | Start Date*: 2015-11-24 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A multicenter, randomized, double-blind, crossover placebo-controlled Phase II study to assess the effect of serelaxin versus placebo on high sensitivity cardiac troponin I (hs-cTnI) release in pat... | |||||||||||||
Medical condition: Chronic Heart Failure | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2007-001994-27 | Sponsor Protocol Number: 2006B180 | Start Date*: 2007-09-03 | |||||||||||
Sponsor Name:Academisch Medisch Centrum | |||||||||||||
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: 2010-020352-59 | Sponsor Protocol Number: GHF112670 | Start Date*: 2010-07-29 | |||||||||||
Sponsor Name:GlaxoSmithKline Research & Development Limited | |||||||||||||
Full Title: A multi-center, placebo-controlled study to evaluate the safety of GSK716155 and its effects on myocardial metabolism, myocardial function, and exercise capacity in patients with NYHA Class II/III ... | |||||||||||||
Medical condition: NYHA Class II/III congestive heart failure. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-000473-20 | Sponsor Protocol Number: CLCZ696B3402 | Start Date*: 2016-08-18 | |||||||||||
Sponsor Name:Novartis Pharma services AG | |||||||||||||
Full Title: A prospective evaluation of natriuretic peptide based referral of CHF patients in primary care | |||||||||||||
Medical condition: Chronic heart failure with reduced ejection fraction | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HR (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-000126-19 | Sponsor Protocol Number: SPIHF-204 | Start Date*: 2016-08-01 | |||||||||||
Sponsor Name:Stealth BioTherapeutics Inc. | |||||||||||||
Full Title: A Phase 2 Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Cardiac and Renal Effects of Short Term Treatment with Elamipretide in Patients Hospitalized with Congestion due to Hear... | |||||||||||||
Medical condition: Congestive heart failure | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: LV (Completed) NL (Completed) ES (Completed) HU (Completed) GB (Completed) BG (Completed) BE (Completed) | |||||||||||||
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 |
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: 2010-019986-27 | Sponsor Protocol Number: RESPIRO | Start Date*: 2010-06-02 | |||||||||||
Sponsor Name:ISTITUTO AUXOLOGICO ITALIANO | |||||||||||||
Full Title: Breathing disorders in heart failure: high altitude hypoxia as a model to define diagnostic tools, therapeutic strategies and gender related differences. | |||||||||||||
Medical condition: Chronic heart failure | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-002236-92 | Sponsor Protocol Number: 9151 | Start Date*: 2011-08-11 | ||||||||||||||||||||||||||||||||||||
Sponsor Name:Maatschap cardiologie Isala klinieken Zwolle | ||||||||||||||||||||||||||||||||||||||
Full Title: Dopamine on top of standard treatment for patients with exacerbation of Heart Failure, at home situation | ||||||||||||||||||||||||||||||||||||||
Medical condition: exacerbation of Heart Failure treated at home | ||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
Trial protocol: NL (Prematurely Ended) | ||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
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: 2012-001700-37 | Sponsor Protocol Number: CELL-004 | Start Date*: 2012-10-03 | |||||||||||
Sponsor Name:Celladon Corporation | |||||||||||||
Full Title: A Phase 2b, Double-Blind, Placebo-Controlled, Multinational, Multicenter, Randomized Study Evaluating the Safety and Efficacy of Intracoronary Administration of MYDICAR® (AAV1/SERCA2a) in Subjects ... | |||||||||||||
Medical condition: Moderate to advanced heart failure (NYHA class II, III or IV) due to systolic dysfunction | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) DE (Completed) GB (Completed) BE (Completed) PL (Completed) NL (Completed) DK (Completed) HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-002168-17 | Sponsor Protocol Number: BAY94-8862/16275 | Start Date*: 2015-12-09 | |||||||||||||||||||||||||||||||
Sponsor Name:Bayer HealthCare AG | |||||||||||||||||||||||||||||||||
Full Title: A multicenter, randomized, double-blind, double-dummy, parallel-group, active-controlled study to evaluate the efficacy and safety of finerenone compared to eplerenone on morbidity and mortality in... | |||||||||||||||||||||||||||||||||
Medical condition: Subjects with chronic heart failure and reduced ejection fraction after recent heart failure decompensation and additional risk factors, either type 2 diabetes mellitus or chronic kidney disease or... | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: SE (Prematurely Ended) DK (Prematurely Ended) IE (Prematurely Ended) CZ (Prematurely Ended) DE (Prematurely Ended) FI (Prematurely Ended) GB (Prematurely Ended) AT (Prematurely Ended) HU (Prematurely Ended) NL (Prematurely Ended) PT (Prematurely Ended) ES (Prematurely Ended) LT (Prematurely Ended) BG (Prematurely Ended) PL (Prematurely Ended) GR (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2022-004186-21 | Sponsor Protocol Number: VICTORID_01 | Start Date*: 2023-09-14 | |||||||||||||||||||||||||||||||
Sponsor Name:Dipartimento di Medicina-DIMED, università di Padova | |||||||||||||||||||||||||||||||||
Full Title: Beneficial effects of vitamin D combined with oral iron supplementation in patients with chronic heart failure and iron deficiency (VICTORID-HF TRIAL) | |||||||||||||||||||||||||||||||||
Medical condition: Chronic heart failure; iron deficiency | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: IT (Trial now transitioned) | |||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-004704-19 | Sponsor Protocol Number: 3200 | Start Date*: 2016-01-14 | |||||||||||
Sponsor Name:King's College London [...] | |||||||||||||
Full Title: Globifer Forte® Oral Haem and Non-haem Iron Supplementation in Heart Failure: A Randomised, DoubleBlind, Placebo Controlled, Double Dummy, Part Mechanistic. | |||||||||||||
Medical condition: Exercise tolerance of Chronic heart failure patients. | |||||||||||||
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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: 2017-004072-59 | Sponsor Protocol Number: 1245-0167 | Start Date*: 2018-04-03 |
Sponsor Name:Boehringer-Ingelheim España, S.A. | ||
Full Title: A phase III randomised, double-blind trial to evaluate the effect of 12 weeks treatment of once daily EMPagliflozin 10 mg compared with placebo on ExeRcise ability and heart failure symptoms, In pa... | ||
Medical condition: Chronic Heart Failure with preserved Ejection Fraction (HFpEF) | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Completed) GR (Completed) PT (Completed) PL (Completed) SE (Completed) NO (Completed) IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-002781-39 | Sponsor Protocol Number: CRLX030A2209 | Start Date*: 2014-05-09 |
Sponsor Name:Novartis Pharma Services AG | ||
Full Title: Prospective, Double-Blind, Multicenter Study Evaluating the Safety of Repeat Doses of IV Serelaxin in Subjects with Chronic Heart Failure | ||
Medical condition: chronic heart failure | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) IT (Completed) FI (Completed) ES (Completed) SE (Completed) NO (Completed) RO (Completed) NL (Completed) CZ (Completed) | ||
Trial results: View results |
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