- Trials with a EudraCT protocol (1,476)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (8)
1,476 result(s) found for: Heart Failure.
Displaying page 8 of 74.
EudraCT Number: 2022-001604-17 | Sponsor Protocol Number: APHP220428 | Start Date*: 2022-11-15 | |||||||||||
Sponsor Name:Assistance Publique - Hôpitaux de Paris | |||||||||||||
Full Title: Effect of Short-Term Prednisone Therapy on C-Reactive Protein Change in Emergency Department Patients With Acute Heart Failure and Elevated Inflammatory Markers | |||||||||||||
Medical condition: Patients With Acute Heart Failure and Elevated Inflammatory Markers in Emergency Department | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-003048-37 | Sponsor Protocol Number: HSJC-CAR-01-2015 | Start Date*: 2015-11-13 |
Sponsor Name:Juan Luis Bonilla Palomas | ||
Full Title: Effect of ?-3 polyunsaturated fatty acids on serum albumin concentration in patients with acute heart failure, hypoalbuminemia, and high inflammatory activity | ||
Medical condition: Heart failure | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2011-002520-40 | Sponsor Protocol Number: 2009/03 | Start Date*: 2010-10-27 | |||||||||||||||||||||
Sponsor Name:CASA DI CURA PRIVATA S.RAFFAELE - PISANA | |||||||||||||||||||||||
Full Title: Carvedilol, ivabradine and their combination in patients with heart failure - the CARVIVA-HF study | |||||||||||||||||||||||
Medical condition: heart failure | |||||||||||||||||||||||
|
|||||||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-021003-24 | Sponsor Protocol Number: 20100754 | Start Date*: 2011-07-28 | |||||||||||
Sponsor Name:Amgen Inc | |||||||||||||
Full Title: A Double-blind, Randomized, Placebo-controlled, Multicenter Study to Evaluate the Safety and Efficacy of IV Infusion Treatment With Omecamtiv Mecarbil in Subjects With Left Ventricular Systolic Dys... | |||||||||||||
Medical condition: Acute heart failure | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GR (Completed) GB (Completed) LT (Completed) FI (Prematurely Ended) SK (Completed) CZ (Completed) HU (Completed) PL (Completed) BE (Completed) IT (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-003586-26 | Sponsor Protocol Number: CV013-020 | Start Date*: 2018-06-12 | ||||||||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | ||||||||||||||||||
Full Title: A Multicenter, Randomized, Double-Blind, Placebo- and Active-Controlled, Cross-over Phase 2 Study of Continuous 5-Hour Intravenous Infusions of BMS-986231 in Patients with Heart Failure and Impaire... | ||||||||||||||||||
Medical condition: Heart failure and impaired systolic function | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) NL (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2005-002109-22 | Sponsor Protocol Number: 02/05/Hü | Start Date*: 2005-12-01 |
Sponsor Name:Medical University of Vienna | ||
Full Title: Comparative Effects of Telmisartan and Candesartan on glucose metabolism in patients with chronic heart failure | ||
Medical condition: both investigated drugs are well established in the treatment of heart failure or hypertension respectively. As the investigateed Patients have this conditions according to the inclusion criteria, ... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-000884-17 | Sponsor Protocol Number: MOME | Start Date*: 2016-07-20 | |||||||||||
Sponsor Name:Dr Alberto Domínguez-Rodríguez | |||||||||||||
Full Title: A multicenter, open-label, randomized of MOrphine and MEperidine in patients admitted for acute heart failure in emergency departments: the MOME study | |||||||||||||
Medical condition: Acute heart failure is the rapid development or change of signs and symptoms of heart failure that requires medical attention and usually leads to patient hospitalization | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-001433-83 | Sponsor Protocol Number: IMPROVE-AHF | Start Date*: 2015-01-15 | |||||||||||
Sponsor Name:Fundación INCLIVA | |||||||||||||
Full Title: Loop Diuretics Dosage in Patients with Acute Heart Failure and Renal Failure: Conventional versus Carbohydrate Antigen 125 guided Strategy | |||||||||||||
Medical condition: Acute Heart Failure | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-022695-31 | Sponsor Protocol Number: 20110204 | Start Date*: 2011-04-12 | ||||||||||||||||
Sponsor Name:Karolinska Institute, Södersjukhuset AB | ||||||||||||||||||
Full Title: Effects on subclinical heartfailure in type 2 diabetic subjects on liraglutide treatment versus glimepiride both in combination with metformin. | ||||||||||||||||||
Medical condition: Type 2 diabetes mellitus and sublinical heart failure | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: SE (Ongoing) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-000764-25 | Sponsor Protocol Number: P-CHF-01 | Start Date*: 2007-05-10 | ||||||||||||||||
Sponsor Name:Pharmacosmos A/S | ||||||||||||||||||
Full Title: A non-comparative open-label study of Iron Oligosaccharide in CHF patients with iron deficiency (either absolute or functional) anaemia and a need for parenteral iron. | ||||||||||||||||||
Medical condition: Patients with anaemia and who have a need for parenteral iron due to either absolute or functional iron deficiency anaemia will be included. Patients may receive concomitant Erythropoeisis Stimulat... | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: SE (Completed) DK (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2016-000404-28 | Sponsor Protocol Number: CRAD001ANO05 | Start Date*: 2016-07-20 | |||||||||||
Sponsor Name:Novartis Norge AS | |||||||||||||
Full Title: 5, 6 or 7 year follow-up control after the SCHEDULE study (SCANDINAVIAN HEART TRANSPLANT EVEROLIMUS DE NOVO STUDY WITH EARLY CNI AVOIDANCE) Title of the original SCHEDULE study: A controlled ran... | |||||||||||||
Medical condition: Heart transplantation | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) DK (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 |
EudraCT Number: 2006-006843-29 | Sponsor Protocol Number: CKI-303 | Start Date*: 2007-06-13 | |||||||||||
Sponsor Name:NovaCardia Inc | |||||||||||||
Full Title: A multicentre, randomized, double-blind, placebo controlled study of the effects of KW-3902 Injectable Emulsion on heart failure signs and symptoms, diuresis, renal function, and clinical outcomes ... | |||||||||||||
Medical condition: Patients being admitted to hospital with heart failure and volume overload requiring IV therapy after experiencing worsening of renal function. | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) IT (Completed) PL (Completed) GR (Completed) BE (Completed) GB (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-003461-17 | Sponsor Protocol Number: 71272 | Start Date*: 2020-01-07 |
Sponsor Name:Amsterdam UMC, location VUmc | ||
Full Title: Pathophysiological relevance of IRON deficiency and related mitochondrial dysfunction in Heart Failure with Preserved Ejection Fraction (IRON-HFpEF) | ||
Medical condition: Heart failure with preserved ejection fraction | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2007-003070-26 | Sponsor Protocol Number: BLO K026 (D-CAN-546) | Start Date*: 2008-08-13 | ||||||||||||||||
Sponsor Name:Takeda Pharma GmbH | ||||||||||||||||||
Full Title: Candesartan “added” therapy for treatment optimization of symptomatic heart failure with diastolic dysfunction in diabetic and hypertensive patients. A randomized, placebo-controlled, double-blind,... | ||||||||||||||||||
Medical condition: Symptomatic heart failure with diastolic dysfunction in diabetic and hypertensive patients | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2018-000802-46 | Sponsor Protocol Number: D169CC00001 | Start Date*: 2018-09-24 |
Sponsor Name:AstraZeneca AB | ||
Full Title: An International, Double-blind, Randomised, Placebo-Controlled Phase IIIb Study to Evaluate the Effect of Dapagliflozin on Reducing CV Death or Worsening Heart Failure in Patients with Heart Failur... | ||
Medical condition: Heart Failure with Preserved Ejection Fraction (HFpEF) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: CZ (Completed) NL (Completed) ES (Ongoing) PL (Completed) HU (Completed) BE (Completed) RO (Ongoing) | ||
Trial results: View results |
EudraCT Number: 2010-018353-36 | Sponsor Protocol Number: FARM8PRTEC | Start Date*: 2010-05-01 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA OSPEDALE NIGUARDA CA` GRANDA (A.O. DI RILIEVO NAZIONALE) | |||||||||||||
Full Title: BeTACTIC Study. Best Therapy After Cardiac Transplantation, the Italian Challenge. A multicenter, prospective, randomized, open-label study to compare the efficacy and safety of Everolimus and Myc... | |||||||||||||
Medical condition: Paitents will be enrolled at least one year after heart transplant | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-001889-16 | Sponsor Protocol Number: CLB-2006 | Start Date*: 2006-03-01 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA SENESE | |||||||||||||
Full Title: Use of clembuterol in patients affected by valvular hearth disease and dilated cardiomyopathy | |||||||||||||
Medical condition: No healthy subjects (patients affected by valvular hearth disease and dilated cardiomyopathy) | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-000068-40 | Sponsor Protocol Number: FAIR-HF2 | Start Date*: 2017-01-27 | |||||||||||
Sponsor Name:University Medical Center Hamburg-Eppendorf | |||||||||||||
Full Title: Intravenous iron in patients with systolic heart failure and iron deficiency to improve morbidity & mortality. Ferric carboxymaltose Assessment of morbidity and mortality in patients with IRon de... | |||||||||||||
Medical condition: Systolic heart failure associated with iron deficiency | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) HU (Completed) PT (Completed) SI (Completed) PL (Completed) IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-003786-20 | Sponsor Protocol Number: S320.2.011 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Solvay Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Double-Blind, Placebo-Controlled, Randomized, Multi-Center, Dose-Finding Study of SLV320, a Selective A1 Adenosine Receptor Antagonist, to Evaluate the Effect on Renal Function and Safety in Subj... | |||||||||||||
Medical condition: Acute Decompensated Heart Failure | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) DK (Prematurely Ended) PL (Prematurely Ended) IT (Prematurely Ended) FR (Completed) | |||||||||||||
Trial results: View results |
Subscribe to this Search
To subscribe to the RSS feed for this search click here
.
This will provide an RSS feed for clinical trials matching your search that have been added or updated in the last 7 days.
To subscribe to the RSS feed for this search click here

Download Options: | |
---|---|
Number of Trials to download: | |
Download Content: | |
Download Format: | |
Note, where multi-state trials are shown in search results, selecting "Full Trial details" will download full information for each of the member states/countries involved in the trial. |
