- Trials with a EudraCT protocol (21)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
21 result(s) found for: Right heart strain.
Displaying page 1 of 2.
EudraCT Number: 2022-000420-38 | Sponsor Protocol Number: 2021-01755 | Start Date*: 2023-09-18 |
Sponsor Name:Universitätsmedizin Göttingen | ||
Full Title: Dapagliflozin in patients with Right Heart Failure (Dapa-RHF) | ||
Medical condition: Right heart failure defined as (criteria a-c must all be fulfilled): a) Reduced right ventricular systolic function or RV strain defined as at least one of the following b) N-terminal pro-BNP (NT... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2006-000021-57 | Sponsor Protocol Number: 01000 | Start Date*: 2006-03-10 |
Sponsor Name:Rigshospitalet | ||
Full Title: Bosentan and Sildenfil for patients with Eisenmenger syndrome | ||
Medical condition: Eisenmengers syndrome is condition with severe pulmonary arterial hypertension due to a shunting of blood from the left side of the heart to the right side of the heart. When the pressure in the pu... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (Completed) | ||
Trial results: View results |
EudraCT Number: 2013-001659-10 | Sponsor Protocol Number: S55481 | Start Date*: 2013-08-08 | |||||||||||
Sponsor Name:UZLeuven | |||||||||||||
Full Title: Acute effects of Sildenafil on the hemodynamics, Right Ventricle performance and cyclic GMP concentration in Heart failure patients with preserved left ventricular ejection fraction and patients af... | |||||||||||||
Medical condition: To investigate acute effects of sildenafil on cardiac hemodynamics, right ventricle performance and cGMP concentrations in heart failure patients with preserved ejection fraction and patients after... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-002835-17 | Sponsor Protocol Number: 250774 | Start Date*: 2016-01-18 | ||||||||||||||||||||||||||
Sponsor Name:Justus Liebig Universität Gießen | ||||||||||||||||||||||||||||
Full Title: Investigation of the influence of PAH-specific medication on right ventricular function in patients with pulmonary arterial hypertension (PAH) under basal conditions | ||||||||||||||||||||||||||||
Medical condition: Pulmonary arterial Hypertension (PAH) | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-000661-20 | Sponsor Protocol Number: ICO | Start Date*: 2019-05-31 |
Sponsor Name:Vilnius University Hospital Santaros klinikos | ||
Full Title: Ivabradine to prevent anthracycline-induced cardiotoxicity: a prospective randomized open label clinical trial. | ||
Medical condition: Cancers treated with anthracyclines: leukemias, limphomas, breast, stomach, uterine, ovarian, lung. | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: LT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2019-002558-21 | Sponsor Protocol Number: AT-001-2001 | Start Date*: 2020-01-15 | |||||||||||
Sponsor Name:Applied Therapeutics Inc. | |||||||||||||
Full Title: Aldose Reductase Inhibition for Stabilization of Exercise capacity in Heart Failure (ARISE-HF): A Multicenter, Randomized, Placebo-Controlled Study to Evaluate the Safety and Efficacy of AT-001 in ... | |||||||||||||
Medical condition: Diabetic Cardiomyopathy (DbCM) / Stage B Heart Failure (SBHF) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) DE (Prematurely Ended) ES (Prematurely Ended) FR (Prematurely Ended) CZ (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2022-000655-36 | Sponsor Protocol Number: 80684 | Start Date*: 2023-04-06 |
Sponsor Name:Amsterdam UMC | ||
Full Title: Evaluation of GeranylGeranylAcetone in heart failure with preserved ejection fraction | ||
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: 2021-000481-14 | Sponsor Protocol Number: APHP210166 | Start Date*: 2021-12-20 |
Sponsor Name:Assistance Publique – Hôpitaux de Paris (AP-HP) | ||
Full Title: Cardiometabolic effects of dapagliflozin in heart failure with reduced ejection fraction: an exploratory study. | ||
Medical condition: Heart failure with reduced ejection fraction | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2018-003564-31 | Sponsor Protocol Number: 190580-001 | Start Date*: 2020-01-16 | |||||||||||
Sponsor Name:Aarhus University Hospital | |||||||||||||
Full Title: Low dose catheter directed thrombolysis for acute intermediary-high risk pulmonary embolism. | |||||||||||||
Medical condition: Acute intermediary-high risk pulmonary embolism | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-002669-37 | Sponsor Protocol Number: GB002-2101 | Start Date*: 2020-10-08 | |||||||||||
Sponsor Name:GB002, Inc. | |||||||||||||
Full Title: A Phase 2, Randomized, Double-Blind, Placebo-Controlled, Multi-Center Clinical Study to Evaluate the Efficacy and Safety of Oral Inhalation of GB002 for the Treatment of WHO Group 1 Pulmonary Arter... | |||||||||||||
Medical condition: Pulmonary Arterial Hypertension (PAH) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) FR (Completed) DE (Completed) AT (Completed) CZ (Completed) BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-001341-27 | Sponsor Protocol Number: Empire-2017 | Start Date*: 2017-05-29 | |||||||||||
Sponsor Name:Morten Schou | |||||||||||||
Full Title: Empagliflozin in heart failure patients with reduced ejection fraction: A randomized clinical trial (Empire HF) | |||||||||||||
Medical condition: Heart failure with reduced ejection fraction | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-006131-10 | Sponsor Protocol Number: APD418-201 | Start Date*: 2021-09-29 | |||||||||||
Sponsor Name:Arena Pharmaceuticals, Inc. | |||||||||||||
Full Title: A Phase 2, Multicenter, Randomized, Double-Blind, Placebo-Controlled Study to Assess the Hemodynamic Effects, Safety, Tolerability, and Pharmacokinetics of APD418 in Subjects with Heart Failure wit... | |||||||||||||
Medical condition: Treatment of acute heart failure with reduced ejection fraction (HFrEF) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-005724-10 | Sponsor Protocol Number: SPIHF-201 | Start Date*: 2016-06-07 | |||||||||||
Sponsor Name:Stealth BioTherapeutics Inc. | |||||||||||||
Full Title: A Phase 2 Randomized, Double-Blinded, Placebo-Controlled Study to Evaluate the Effects of Multiple Subcutaneous Injections of Elamipretide on Left Ventricular Function in Subjects with Stable Heart... | |||||||||||||
Medical condition: Stable Heart Failure with Reduced Ejection Fraction | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) GB (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-006787-25 | Sponsor Protocol Number: 16122021 | Start Date*: 2022-07-06 | |||||||||||||||||||||||||||||||
Sponsor Name:Rigshospitalet The Heart Center | |||||||||||||||||||||||||||||||||
Full Title: Effects of DAPAgliflozin on cardiopulmonary exercise capacity and hemodynamics in Pulmonary Arterial Hypertension: A double blind randomized trial | |||||||||||||||||||||||||||||||||
Medical condition: Pulmonary arterial hypertension Chronic thromboembolic pulmonary hypertension | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: DK (Trial now transitioned) | |||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-000130-33 | Sponsor Protocol Number: ORION-HF | Start Date*: 2022-12-23 | ||||||||||||||||||||||||||
Sponsor Name:Hannover Medical School | ||||||||||||||||||||||||||||
Full Title: A pilot study to explore safety, tolerability and efficacy of ORal IrON supplementation with ferric maltol in treating iron deficiency and anaemia in patients with Heart Failure (ORION-HF) | ||||||||||||||||||||||||||||
Medical condition: Patients with heart failure, iron deficiency and anaemia with either reduced or preserved left ventricular ejection fraction | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-001617-21 | Sponsor Protocol Number: 72864 | Start Date*: 2020-08-27 |
Sponsor Name:Aarhus University Hospital | ||
Full Title: The Effect of Trimetazidine on Mitochondrial Function, Myocardial Performance, and Invasive Hemodynamics in Patients Diagnosed with Wild-Type Transthyretin Cardiac Amyloidosis. | ||
Medical condition: Wild-Type Transthyretin Cardiac Amyloidosis | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: DK (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-004783-22 | Sponsor Protocol Number: 67896049PAH4005 | Start Date*: 2020-12-03 | |||||||||||
Sponsor Name:ACTELION Pharmaceuticals Ltd. | |||||||||||||
Full Title: A PRospective, Multicenter, Single-arm, Open label, Phase 4 Study of the Effects of Selexipag on RighT Ventricular RemOdeling in Pulmonary Arterial Hypertension Assessed by Cardiac Magnetic REsonan... | |||||||||||||
Medical condition: Pulmonary Arterial Hypertension | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) DE (Completed) GB (GB - no longer in EU/EEA) FR (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-003497-48 | Sponsor Protocol Number: EMPATHY | Start Date*: 2021-11-29 | |||||||||||
Sponsor Name:Medical University of Warsaw | |||||||||||||
Full Title: Empagliflozin and dapagliflozin in patients hospitalized for acute decompensated heart failure (EMPATHY) – a phase III trial | |||||||||||||
Medical condition: acute decompensated heart failure | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-006953-77 | Sponsor Protocol Number: 27-12-2021 | Start Date*: 2022-04-11 | ||||||||||||||||||||||||||
Sponsor Name:Aarhus University Hospital | ||||||||||||||||||||||||||||
Full Title: Treatment effects of Bisoprolol and Verapamil in symptomatic patients with non-obstructive hypertrophic cardiomyopathy | ||||||||||||||||||||||||||||
Medical condition: Non-obstructive Hypertrophic cardiomyopathy | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: DK (Trial now transitioned) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-000927-42 | Sponsor Protocol Number: HZC116601 | Start Date*: 2012-10-19 | |||||||||||
Sponsor Name:GlaxoSmithKline Research and Development Ltd | |||||||||||||
Full Title: A Randomised, Double-Blind, Placebo-Controlled, Cross-Over, Single-Centre Study to Investigate the Acute Lung Deflation Effects of Fluticasone Furoate/Vilanterol Inhalation Powder 100/25mcg Once Da... | |||||||||||||
Medical condition: Chronic Obstructive Pulmonary Disease (COPD) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
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