- Trials with a EudraCT protocol (6)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
6 result(s) found for: ,DHF.
Displaying page 1 of 1.
| EudraCT Number: 2006-002605-31 | Sponsor Protocol Number: Aldo-DHF | Start Date*: 2007-02-01 | |||||||||||
| Sponsor Name:Georg-August-Universität Göttingen | |||||||||||||
| Full Title: ALDOSTERONE RECEPTOR BLOCKADE IN DIASTOLIC HEART FAILURE A double-blind, randomised, placebo-controlled, parallel group study to determine the effects of spironolactone on exercise capacity and dia... | |||||||||||||
| Medical condition: Diastolic Heart Failure | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) AT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-002546-49 | Sponsor Protocol Number: SCP-01-001 | Start Date*: 2014-10-03 |
| Sponsor Name:scPharmaceuticals Inc | ||
| Full Title: A single center, randomized, open-label, cross-over exploratory study to evaluate the pharmacodynamic and pharmacokinetic response to a subcutaneous administration or oral administration of furosem... | ||
| Medical condition: Fluid overload in heart failure | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: NL (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2010-018436-41 | Sponsor Protocol Number: Bay 63-2521/14554 | Start Date*: 2010-05-11 | |||||||||||
| Sponsor Name:Bayer HealthCare AG | |||||||||||||
| Full Title: Acute hemoDynamic effects of RIociguat (BAY 63-2521) in patients with puLmonary hypertension Associated with diasTolic heart failurE (DILATE 1): A randomized, double-blind, placebo-controlled, sin... | |||||||||||||
| Medical condition: Pulmonary hypertension associated with diastolic heart failure | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: AT (Prematurely Ended) CZ (Prematurely Ended) DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-003601-25 | Sponsor Protocol Number: DROP-PIP | Start Date*: 2014-03-28 |
| Sponsor Name:Charité Universitätsmedizin Berlin | ||
| Full Title: A multicenter, Double-blind, RandOmised, two arm Parallel group trial to determine the effects of torasemide versus furosemide on one marker (PIP) of cardiac fibrosis in patient with Diastolic Hear... | ||
| Medical condition: Diastolic heart failure and diabetes mellitus type II | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2015-003146-75 | Sponsor Protocol Number: BETA3_LVH | Start Date*: 2016-03-14 | |||||||||||
| Sponsor Name:Université catholique de Louvain (UCL) | |||||||||||||
| Full Title: A multi-centre randomized, placebo-controlled trial of mirabegron, a new beta3-adrenergic receptor agonist on the progression of left ventricular mass and diastolic function in patients with struct... | |||||||||||||
| Medical condition: Structural heart disease at high risk for progressive hypertrophic cardiac remodeling at risk of developing HFpEF (heart failure with preserved ejection fraction). | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) DE (Completed) PT (Completed) GR (Completed) PL (Completed) FR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| 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 | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DE (Prematurely Ended) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
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