- Trials with a EudraCT protocol (159)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
159 result(s) found for: Beta blockers.
Displaying page 1 of 8.
EudraCT Number: 2021-001905-66 | Sponsor Protocol Number: BA-SCAD | Start Date*: 2021-07-06 |
Sponsor Name:Spanish Cardiology Society | ||
Full Title: Randomized clinical trial assessing the value of Beta-Blockers and Antiplatelet Agents in patients with Spontaneous Coronary Artery Dissection | ||
Medical condition: Spontaneous Coronary Artery Dissection | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2006-003991-37 | Sponsor Protocol Number: AGO/2006/009 | Start Date*: 2006-12-13 | |||||||||||
Sponsor Name:University Hospital Gent | |||||||||||||
Full Title: Trial of beta blocker therapy (atenolol) vs. angiotensin II receptor blocker therapy (losartan) in individuals with Marfan syndrome | |||||||||||||
Medical condition: Marfan syndrome | |||||||||||||
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Population Age: Infants and toddlers, Children, Adolescents, Under 18, Adults | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-002207-15 | Sponsor Protocol Number: Cardiorete | Start Date*: 2011-12-27 |
Sponsor Name:FONDAZIONE DEL PIEMONTE PER L'ONCOLOGIA IRCC DI CANDIOLO | ||
Full Title: A prospective study with beta-blockers and ACE-inhibitors in patients operable breast cancer experiencing mild cardiac toxicity during treatment with anthracycline and/or trastuzumab | ||
Medical condition: patients experiencing mild cardiotoxicity during treatment with anthracycline and/or trastuzumab for operable breast cancer | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Female | |
Trial protocol: IT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2014-002037-59 | Sponsor Protocol Number: CSPH-EX-0414 | Start Date*: 2015-04-01 |
Sponsor Name:Exalenz BioScience Ltd. | ||
Full Title: Clinical Study of the BreathID® LF System to train the algorithm for the ¹³C-Methacetin Breath Test (MBT) in assessment of Portal Hypertension in Patients with Compensated Liver Cirrhosis | ||
Medical condition: Compensated Liver Cirrhosis and indication to undergo HVPG testing | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-000701-35 | Sponsor Protocol Number: ERASMUS2006,Sofia1 | Start Date*: 2006-03-14 |
Sponsor Name:Erasmus Hospital | ||
Full Title: Chemoreflex sensitivity during exercise with beta blockers | ||
Medical condition: Sportive individuals, athletes | ||
Disease: | ||
Population Age: Adults | Gender: Male | |
Trial protocol: BE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2014-000102-35 | Sponsor Protocol Number: 35128 | Start Date*: 2014-12-19 |
Sponsor Name:Clinica Medica 5 | ||
Full Title: Effect of administration "add on" of Rifaximin on portal hypertension of patients with liver cirrhosis and esophageal varices in standard therapy with propranolol | ||
Medical condition: Portal hypertension, liver cirrhosis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IT (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2011-004192-37 | Sponsor Protocol Number: CRO1749 | Start Date*: 2012-04-24 | |||||||||||
Sponsor Name:Joint Research Compliance Office, Imperial College | |||||||||||||
Full Title: Hellenic Anglo Research into Morning Or Night antihypertensive drug deliverY trial. | |||||||||||||
Medical condition: Hypertension | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-001507-76 | Sponsor Protocol Number: BRONCHIOLE2017 | Start Date*: 2017-09-20 |
Sponsor Name:Region Örebro län | ||
Full Title: Beta-blockeRs tO patieNts with CHronIc Obstructive puLmonary diseasE (BRONCHIOLE) A pragmatic clinical trial with partial registry-based follow-up | ||
Medical condition: Chronic Obstructive Pulmonary disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2007-002431-80 | Sponsor Protocol Number: LEV1068 | Start Date*: 2006-09-15 | |||||||||||
Sponsor Name:AZIENDA UNIVERSITARIA POLICLINICO UMBERTO I DI ROMA | |||||||||||||
Full Title: Renal Effects of Levosimendan in Patients Admitted with Acute Decompensated Heart Failure | |||||||||||||
Medical condition: Patients with acute decompensated heart failure. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-003568-20 | Sponsor Protocol Number: RGR | Start Date*: 2008-08-08 |
Sponsor Name:Prof Alice Stanton | ||
Full Title: Renin Genotype and Response to Renin Angiotensin System Blockade. | ||
Medical condition: Hypertension | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IE (Completed) | ||
Trial results: View results |
EudraCT Number: 2017-002336-17 | Sponsor Protocol Number: REDUCe_2017-05-22 | Start Date*: 2017-08-06 |
Sponsor Name:Department of Clinical Sciences, Danderyd Hospital, Karolinska Intitutet | ||
Full Title: Randomized Evaluation of Decreased Usage of betablocCkErs after myocardial infarction in the SWEDEHEART registry REDUCe SWEDEHEART | ||
Medical condition: Long-term treatment with beta-blockers in patients with myocardial infarction and preserved ejection fraction. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) EE (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-006793-28 | Sponsor Protocol Number: CL3-16257-078 | Start Date*: 2008-09-18 | |||||||||||
Sponsor Name:Institut de Recherches Internationales Servier (I.R.I.S) | |||||||||||||
Full Title: Effects of a 10 or 15 mg single intravenous bolus of ivabradine versus placebo on heart rate control during a multislice computed tomography coronary angiography for the evaluation of coronary arte... | |||||||||||||
Medical condition: Heart rate control during a MultiSlice Computed Tomography Coronary Angiography (MST CA) for the evaluation of Coronary Artery Disease | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) GB (Completed) BE (Completed) PT (Completed) HU (Completed) ES (Completed) DE (Completed) FR (Completed) DK (Completed) IT (Completed) PL (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-001037-72 | Sponsor Protocol Number: ABR60023 | Start Date*: 2017-12-01 |
Sponsor Name:Leiden University Medical Center | ||
Full Title: The efficacy of flEcainide Compared To metOprolol in reducing Premature ventrIcular Complexes. An open label cross-over study in pediatric patients. | ||
Medical condition: frequent premature ventricular contractions | ||
Disease: | ||
Population Age: Infants and toddlers, Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2004-002754-62 | Sponsor Protocol Number: 2004-001 | Start Date*: 2006-06-20 |
Sponsor Name:University of Göttingen; Dep. of Clinical Pharmacology | ||
Full Title: Development of CYP2D6 genotype based dosage guidelines for the beta-blockers metoprolol and carvedilol based on hepatic clearance and resting and exercise heart rate reduction | ||
Medical condition: Healthy male and female volunteers | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2014-002018-21 | Sponsor Protocol Number: FOL12-01 | Start Date*: 2015-02-10 | ||||||||||||||||
Sponsor Name:AOU di Bologna Policlinico S.Orsola-Malpighi | ||||||||||||||||||
Full Title: 5-Metyl-tetrahydrofolate in the treatment of portal hypertension in cirrhotics in pharmacologic prophylaxis of variceal bleeding with beta-blockers: a double-blind randomized controlled trial | ||||||||||||||||||
Medical condition: portal hypertension in cirrhotic patients | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-001793-21 | Sponsor Protocol Number: CPA12001 | Start Date*: 2013-08-06 | |||||||||||
Sponsor Name:PHARMATHEN S.A. | |||||||||||||
Full Title: Efficacy and tolerability of brinzolamide in patients with elevated intraocular pressure: a double-blind, randomized, parallel, verum-controlled trial. | |||||||||||||
Medical condition: intraocular pressure increased | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) GR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-011156-21 | Sponsor Protocol Number: CCFM 119/209 | Start Date*: 2011-04-28 | |||||||||||
Sponsor Name:FONDAZIONE MONZINO CENTRO CARDIOLOGICO | |||||||||||||
Full Title: Effects of beta-blockers on exercise performance in uncomplicated hypertension | |||||||||||||
Medical condition: Non complicated arterial hypertension | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-000103-34 | Sponsor Protocol Number: CL2-16257-062 | Start Date*: 2005-07-13 | |||||||||||
Sponsor Name:Institut de Recherches Internationales Servier [...] | |||||||||||||
Full Title: Evaluation of the effects of 3 successive oral dosages (2.5; 5; 7.5 mg b.i.d.) of ivabradine in patients with stable moderate to severe systolic chronic heart failure treated with beta-blockers. A ... | |||||||||||||
Medical condition: Chronic systolic heart failure | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-006008-11 | Sponsor Protocol Number: ANDA2 | Start Date*: 2012-08-22 | |||||||||||
Sponsor Name:Tayside Clinical Trials Unit, University of Dundee | |||||||||||||
Full Title: Evaluation of effects of chronic dose exposure to cardioselective and non-cardioselective beta blockers on measures of cardiopulmonary function in moderate to severe COPD. | |||||||||||||
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 |
EudraCT Number: 2008-001509-40 | Sponsor Protocol Number: BETAVASC-IV-08-1 | Start Date*: 2008-10-18 |
Sponsor Name:Hungarian Kidney Foundation | ||
Full Title: Effects of beta blockers on central arterial pressure and vascular stiffness | ||
Medical condition: Patients with hypertension and/or ischemic heart disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: HU (Completed) | ||
Trial results: (No results available) |
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