- Trials with a EudraCT protocol (84)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
84 result(s) found for: Doppler echocardiography.
Displaying page 1 of 5.
EudraCT Number: 2007-000467-23 | Sponsor Protocol Number: 1 | Start Date*: 2007-08-23 | ||||||||||||||||||||||||||
Sponsor Name:Erasmus MC | ||||||||||||||||||||||||||||
Full Title: Maternal and fetal haemodynamic response to Nifedipine tocolysis in normotensive pregnant women. | ||||||||||||||||||||||||||||
Medical condition: A more detailed investigation of the haemodynamic effect on the mother and fetus of Nifedipine tocolysis . Tocolysis will be used to facilitate external cephalic version for breech presentation at ... | ||||||||||||||||||||||||||||
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Population Age: In utero, Under 18, Adults | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: NL (Completed) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-000727-17 | Sponsor Protocol Number: 281274 | Start Date*: 2007-08-23 | ||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:Erasmus MC | ||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: Maternal, uteroplacental and fetal haemodynamic effect of Nicardipine in severe pre-eclampsia. | ||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Hypertensive crisis in patients with severe pre-eclampsia needs to be treated to prevent maternal and fetal complications. The maternal, uteroplacental and fetal haemodynamic respose to antihypert... | ||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Female | |||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: NL (Completed) | ||||||||||||||||||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-002332-15 | Sponsor Protocol Number: D1840M00006 | Start Date*: 2008-09-15 |
Sponsor Name:AstraZeneca AB | ||
Full Title: A randomised, double-blind, placebo-controlled study to evaluate the transthoracic Doppler echocardiography method as a non-invasive method for coronary function measurements; ability to detect sho... | ||
Medical condition: In this study the IMP, rosuvastatin, is used as a tool compound for creating favourable lipid-altering, anti-inflammatory or other pleiotropic effects which are believed to change coronary flow res... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-002293-54 | Sponsor Protocol Number: Apex01version6 | Start Date*: 2007-11-29 |
Sponsor Name:University of Dundee | ||
Full Title: The APEX Trial: Effects of Allopurinol on Coronary and Peripheral Endothelial Function in Patients with Cardiac Syndrome X | ||
Medical condition: Patients with cardiac syndrome X (typical anginal-like chest pain and normal coronary arteriograms) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2010-021664-16 | Sponsor Protocol Number: SVUH | Start Date*: 2010-11-04 | |||||||||||
Sponsor Name:Solvotrin Innovations Ltd | |||||||||||||
Full Title: The role of doxycycline in the management of diastolic dysfunction | |||||||||||||
Medical condition: Diastolic dysfunction | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Completed) | |||||||||||||
Trial results: Removed from public view |
EudraCT Number: 2015-003521-34 | Sponsor Protocol Number: CHUBX2015/14 | Start Date*: 2015-10-09 |
Sponsor Name:CHU de Bordeaux | ||
Full Title: Hypertrophic CARdiomyopathy symptom release by alpha stimulant MIDOdrine | ||
Medical condition: Hypertrophic cardiomyopathy | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2015-002928-53 | Sponsor Protocol Number: HBT-GCP-PTCL-01 | Start Date*: 2015-11-16 |
Sponsor Name:The Heartbeat Trust | ||
Full Title: Personalised prospective comparison of ARni with ArB in patients with natriuretic peptide eLEvation (PARABLE) | ||
Medical condition: Patients (asymptomatic) with cardiovascular risk factors for heart failure including either hypertension and/or type II diabetes, with elevated levels of natriuretic peptide (brain natriuretic pept... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IE (Completed) | ||
Trial results: View results |
EudraCT Number: 2019-004427-20 | Sponsor Protocol Number: CHHEF | Start Date*: 2020-02-07 | |||||||||||
Sponsor Name:Luis Puente Maestu | |||||||||||||
Full Title: PHASE IV, SINGLE-CENTER, DOUBLE BLIND, RANDOMIZED, CROSSOVER, PLACEBO-CONTROLLED STUDY, TO INVESTIGATE THE EFFECT OF DUAL BRONCHODILATION WITH UMECLIDINIUM VILANTEROL ON PATIENTS WITH COPD, HYPERIN... | |||||||||||||
Medical condition: Chronic obstructive pulmonary diseases with Heart Failure with eyection ventricular ejection fraction between 35-50% | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2009-016096-29 | Sponsor Protocol Number: 08/0183 | Start Date*: 2010-03-05 |
Sponsor Name:University College London [...] | ||
Full Title: Pilot of oral Sildenafil for the treatment of Pulmonary Hypertension in Thalassaemia with comparison to controls. | ||
Medical condition: Pulmonary Hypertension in Thalassaemia patients | ||
Disease: | ||
Population Age: Adolescents, Under 18, Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2017-000240-17 | Sponsor Protocol Number: ESTIMATE | Start Date*: 2017-05-02 | |||||||||||
Sponsor Name:Bispebjerg University Hospital | |||||||||||||
Full Title: Effect of SGLT2 inhibition on coronary microvascular function in type 2 diabetes | |||||||||||||
Medical condition: Coronary microvascular function in patients with type 2 diabetes | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-001930-34 | Sponsor Protocol Number: 170674-3479 | Start Date*: 2005-11-25 |
Sponsor Name:Department of Cardiology, Odense University Hospital | ||
Full Title: Left ventricular reverse remodelling after aortic valve replacement in severe valvular aortic stenosis - effect of blockade of the angiotensin-II receptor | ||
Medical condition: Patients with severe aortic valve stenosis treated with Aortic Valve Replacement (AVR) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2009-009871-36 | Sponsor Protocol Number: 140/540 | Start Date*: Information not available in EudraCT |
Sponsor Name:Friedrich- Alexander- Universität Erlangen Nürnberg | ||
Full Title: Effect and Safety of preventive Treatment with ACE-Inhibitor and Beta-Blocker on the onset of Left Ventricular Dysfunction in Duchenne Muscular Dystrophy | ||
Medical condition: | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male | |
Trial protocol: DE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2009-017168-17 | Sponsor Protocol Number: GS-US-270-0101 | Start Date*: 2010-05-31 | |||||||||||
Sponsor Name:Gilead Sciences, Inc. | |||||||||||||
Full Title: A Randomized, Double-blind, Placebo-controlled Study of Ranolazine in Patients with Heart Failure with Preserved Ejection Fraction | |||||||||||||
Medical condition: Heart failure with Preserved Ejection Fraction | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2015-004498-34 | Sponsor Protocol Number: SUM | Start Date*: 2016-12-12 | |||||||||||
Sponsor Name:UMBERTO I - POLICLINICO DI ROMA | |||||||||||||
Full Title: Study on New Insights in Remodeling of Endocrine Cardiomyopathies: ASsessmentt of Intramyocardial, Molecular and NeUroendocrine Parameters in Response to Chronic Inhibition of Cyclic GMP Phosphodie... | |||||||||||||
Medical condition: Acromegaly | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-002020-25 | Sponsor Protocol Number: 052017 | Start Date*: 2018-08-31 | |||||||||||
Sponsor Name:Odense University Hospital | |||||||||||||
Full Title: ANGIOTENSIN–NEPRILYSIN INHIBITION IN DIASTOLIC DYSFUNCTION AFTER AMI | |||||||||||||
Medical condition: Diastolic dysfunction after acute myocardial infarction | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-002571-33 | Sponsor Protocol Number: 49RC19_0106 | Start Date*: 2019-08-28 |
Sponsor Name:CHU Angers | ||
Full Title: Transcutaneous measurement of oxygen during transient hyperoxia | ||
Medical condition: Any patient with a cardiac output measurement | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Completed) | ||
Trial results: View results |
EudraCT Number: 2017-002530-23 | Sponsor Protocol Number: MYK-461-005 | Start Date*: 2018-10-04 | |||||||||||
Sponsor Name:MyoKardia, Inc. | |||||||||||||
Full Title: A Randomized, Double blind, Placebo controlled Clinical Study to Evaluate Mavacamten (MYK-461) in Adults with Symptomatic Obstructive Hypertrophic Cardiomyopathy | |||||||||||||
Medical condition: Hypertrophic Cardiomyopathy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) GB (Completed) PT (Completed) ES (Completed) CZ (Completed) BE (Completed) NL (Completed) PL (Completed) DK (Completed) FR (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-001922-26 | Sponsor Protocol Number: BMI-EU-02-008 | Start Date*: 2006-01-06 |
Sponsor Name:Bioheart, Inc | ||
Full Title: A Phase II, Open-label, Randomized, Multicenter Study to Assess the Safety and Cardiovascular Effects of MyoCell™ Implantation by a Catheter Delivery System in Congestive Heart Failure Patients Pos... | ||
Medical condition: Patients with congestive heart failure who have had a previous myocardial infarction. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2014-003273-42 | Sponsor Protocol Number: 14AOI11 | Start Date*: 2014-12-23 | |||||||||||
Sponsor Name:CHU de Nice | |||||||||||||
Full Title: Comparing a diuretic vascular filling in the initial management of acute pulmonary embolism with right ventricular dysfunction normotensive | |||||||||||||
Medical condition: acute pulmonary embolism with right ventricular dysfunction normotensive | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-000540-26 | Sponsor Protocol Number: CVT-CV-002 | Start Date*: 2013-05-12 | |||||||||||
Sponsor Name:CVie Therapeutics Company Limited | |||||||||||||
Full Title: The clinical study of the safety and efficacy of Istaroxime in Treatment of Acute Decompensated Heart Failure - A multicenter, randomized, double-blind, placebo controlled, parallel group clinical ... | |||||||||||||
Medical condition: Acute heart failure decompensated | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
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