- Trials with a EudraCT protocol (101)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
101 result(s) found for: Hypertensive heart disease.
Displaying page 1 of 6.
EudraCT Number: 2009-012624-93 | Sponsor Protocol Number: BREVI | Start Date*: 2009-06-08 | |||||||||||
Sponsor Name:OSPEDALE S. RAFFAELE | |||||||||||||
Full Title: Esmolol in cardiac surgery. A randomized controlled trial with clinical relevant endpoints. | |||||||||||||
Medical condition: patients undergoing cardiac surgery | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-001616-31 | Sponsor Protocol Number: OLM/CLIN/I-12/03 | Start Date*: 2005-05-27 | |||||||||||
Sponsor Name:LUSOFARMACO [...] | |||||||||||||
Full Title: EFFICACY AND SAFETY OF OLMESARTAN IN ELDERLY PATIENTS WITH MILD TO MODERATE HYPERTENSION | |||||||||||||
Medical condition: patients of both sexes, aged 65-89 years and with mild-moderate essential arterial hypertension | |||||||||||||
|
|||||||||||||
Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-024448-13 | Sponsor Protocol Number: 010884 | Start Date*: 2011-02-18 | |||||||||||
Sponsor Name:Netherlands Heart Foundation | |||||||||||||
Full Title: Effects of low-dose aspirin taken at bedtime on blood pressure of subjects with who use aspirin for prevention of recurrent cardiovascular events: the Aspirin In Reduction of Tension II (ASPIRETENS... | |||||||||||||
Medical condition: The medical condition to be investigated is hypertension | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-000310-36 | Sponsor Protocol Number: 2542 | Start Date*: 2007-04-05 | |||||||||||
Sponsor Name:Radboud University Medical Center Njmegen | |||||||||||||
Full Title: Does statin therapy reduce sympathoexcitation in hypertension | |||||||||||||
Medical condition: hypertension and sympathoexcitation | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-003676-22 | Sponsor Protocol Number: TMC-CLV-08-01 | Start Date*: 2009-04-01 | ||||||||||||||||
Sponsor Name:The Medicines Company | ||||||||||||||||||
Full Title: A Safety and Efficacy Study of Blood Pressure Control in Acute Heart Failure – A Pilot Study (PRONTO) | ||||||||||||||||||
Medical condition: acute heart failure and elevated BP (systolic blood pressure [SBP] ≥160 mm Hg) requiring parenteral IV antihypertensive therapy | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-004760-29 | Sponsor Protocol Number: UIAPB-TAHPS-2011-01 | Start Date*: 2012-01-16 | |||||||||||
Sponsor Name:Maria Victoria Ruiz Arzalluz | |||||||||||||
Full Title: EFFECTIVENESS OF ADMINISTRATION TIMING OF ASPIRIN FROM DAYTIME TO NIGHTIME IN HYPERTENSIVE PATIENTS TREATED WITH LOW DOSE OF ASA IN SECONDARY PREVENTION. - TAHPS | |||||||||||||
Medical condition: hypertension | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-005484-31 | Sponsor Protocol Number: 20-197 | Start Date*: 2022-10-07 | |||||||||||
Sponsor Name:CHU CAEN Normandie | |||||||||||||
Full Title: SPironolactONe for the maintenance of Sinus Rhythm in hypertensive patients with atrial fibrillation and preserved left ventricular ejection fraction: a Prospective Randomized Open Blinded End-poin... | |||||||||||||
Medical condition: Hypertensive patients > 18 years referred for documented AF episodes (symptomatic or not) with preserved left ventricular ejection fraction (LVEF). | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-005401-22 | Sponsor Protocol Number: 24092007 | Start Date*: 2009-02-20 |
Sponsor Name:University Medical Center Utrecht | ||
Full Title: Effect of Aliskiren on Muscle Sympathetic Nerve Activity in hypertensive patients with chronic kidney disease | ||
Medical condition: Hypertension and chronic kidney disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2006-004794-10 | Sponsor Protocol Number: A3841047 | Start Date*: 2006-12-14 | |||||||||||
Sponsor Name:Pfizer Limited | |||||||||||||
Full Title: A CLUSTER RANDOMIZED TRIAL ON CARDIOVASCULAR RISK FACTOR MANAGEMENT: CADUET® VERSUS USUAL CARE IN SUBJECTS WITH HYPERTENSION AND ADDITIONAL CARDIOVASCULAR RISK FACTORS IN CLINICAL PRACTICE | |||||||||||||
Medical condition: HYPERTENSION AND ADDITIONAL CARDIOVASCULAR RISK FACTORS. | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-004188-35 | Sponsor Protocol Number: CCM1140 | Start Date*: 2020-10-07 | |||||||||||
Sponsor Name:CENTRO CARDIOLOGICO SPA FONDAZIONE MONZINO | |||||||||||||
Full Title: Time-dependent activity of N-acetylcysteine on plasma antioxidant capacity in subjects with redox unbalance-Studio CAPITAL | |||||||||||||
Medical condition: ARTERIAL HYPERTENSION | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-001311-30 | Sponsor Protocol Number: CVAH631BDE13 | Start Date*: 2006-06-23 | |||||||||||
Sponsor Name:Novartis Pharma GmbH | |||||||||||||
Full Title: An open-label, multicenter study to evaluate the efficacy and tolerability of a 4 week therapy with the fixed dose combination of valsartan 160 mg plus HCTZ 25 mg in hypertensive patients not adequ... | |||||||||||||
Medical condition: Moderate essential hypertension (WHO grade II) | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-024175-58 | Sponsor Protocol Number: kardioIKEM2010 | Start Date*: 2011-06-30 | ||||||||||||||||
Sponsor Name:IKEM | ||||||||||||||||||
Full Title: Comparison of two treatment options for hypertension in heart transplant recipients | ||||||||||||||||||
Medical condition: Compensation of arterial hypertension in heart transplant recipients. Renal function and its changes in heart transplant recipients. | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: CZ (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-003131-23 | Sponsor Protocol Number: DSE-866/47 | Start Date*: 2008-07-28 | ||||||||||||||||
Sponsor Name:DAIICHI SANKYO EUROPE GmbH | ||||||||||||||||||
Full Title: Effect of Olmesartan Medoxomil on Arterial Stiffness and Thickness in Subjects with Metabolic Syndrome | ||||||||||||||||||
Medical condition: Metabolic Syndrome, Hypertension | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: BE (Completed) FR (Completed) DE (Completed) GB (Completed) IT (Completed) NL (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-019874-34 | Sponsor Protocol Number: PPT01 | Start Date*: 2010-11-05 | ||||||||||||||||
Sponsor Name:Queen Mary University of London | ||||||||||||||||||
Full Title: A randomised, placebo controlled, double-blind, cross-over trial of the Polypill on risk factor reduction | ||||||||||||||||||
Medical condition: Hypercholesterolaemia and Hypertension | ||||||||||||||||||
|
||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2007-000320-40 | Sponsor Protocol Number: SLx-2101-07-05 | Start Date*: 2007-06-14 | |||||||||||
Sponsor Name:Surface Logix, Inc. | |||||||||||||
Full Title: A pilot Phase IIa randomised, double blind, placebo-controlled, crossover study to examine the safety, tolerability and pharmacodynamic effects on blood pressure of repeat oral doses of SLx-2101 5,... | |||||||||||||
Medical condition: Hypertension | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-007149-30 | Sponsor Protocol Number: 4500 | Start Date*: 2009-01-14 | |||||||||||
Sponsor Name:Cambridge University Hospitals NHS Foundation Trust and University of Cambridge [...] | |||||||||||||
Full Title: Optimal Treatment of Drug Resistant Hypertension | |||||||||||||
Medical condition: Hypertension | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-003407-17 | Sponsor Protocol Number: CLD-1-2021 | Start Date*: 2022-04-19 | |||||||||||
Sponsor Name:University Clinic of Nephrology and Hypertension | |||||||||||||
Full Title: Combined effects of potassium, nitrate and sodium on blood pressure in patients with hypertension | |||||||||||||
Medical condition: Essential Hypertension | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-001374-87 | Sponsor Protocol Number: CVAA489ADE06 | Start Date*: 2007-07-17 | |||||||||||
Sponsor Name:Novartis Pharma GmbH | |||||||||||||
Full Title: An open-label, multicenter study to evaluate the efficacy and tolerability of a 4 week therapy with the fixed dose combination of amlodipine 10 mg plus valsartan 160 mg in hypertensive patients not... | |||||||||||||
Medical condition: essential hypertension | |||||||||||||
|
|||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2010-023206-12 | Sponsor Protocol Number: FARM6HCEM5 | Start Date*: 2008-09-26 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA VINCENZO MONALDI DI NAPOLI | |||||||||||||
Full Title: Arterial Hypertension After Successful Aortic Decoarctation: Atenolol vs Enalapril Comparison of Efficacy and Tolerability in Pediatric Age. | |||||||||||||
Medical condition: Aortic coarctation and hypertensive patients | |||||||||||||
|
|||||||||||||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2013-003204-40 | Sponsor Protocol Number: PATHBP_2013 | Start Date*: 2014-01-20 | ||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:University of Edinburgh [...] | ||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: Paracetamol treatment in hypertension: effect on blood pressure | ||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Hypertension | ||||||||||||||||||||||||||||||||||||||||||||||||
|
||||||||||||||||||||||||||||||||||||||||||||||||
Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: GB (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. |
