- Trials with a EudraCT protocol (527)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
527 result(s) found for: Systemic hypertension.
Displaying page 1 of 27.
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 | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-017831-16 | Sponsor Protocol Number: 26169 | Start Date*: 2010-07-15 | |||||||||||||||||||||||||||||||
Sponsor Name:Institute of pharmacology, Aarhus university | |||||||||||||||||||||||||||||||||
Full Title: Effects of 6 months intensive vasodilating treatment on vascular resistance and coronary flow reserve in hypertensive patients | |||||||||||||||||||||||||||||||||
Medical condition: Essential Hypertension and changes in the vasculature related to high blood pressure. | |||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
Trial protocol: DK (Completed) | |||||||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-000077-22 | Sponsor Protocol Number: CL2-90652-001 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Institut de Recherches Internationales Servier | |||||||||||||
Full Title: Acceptability, safety, pharmacokinetics and effects on blood pressure of a daily dose of 0.025 to 0.135 milligram per kilogram of S 90652, a paediatric formulation of perindopril, in 2-16 years old... | |||||||||||||
Medical condition: Arterial hypertension | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-004411-22 | Sponsor Protocol Number: CSPP100A2365E2 | Start Date*: 2012-03-14 | ||||||||||||||||
Sponsor Name:Novartis Pharma Services AG | ||||||||||||||||||
Full Title: A multicenter, 52 to 104 week extension study to evaluate the long term growth and development of pediatric hypertensive patients 6 – 17 years of age treated previously with aliskiren | ||||||||||||||||||
Medical condition: Hypertension | ||||||||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |||||||||||||||||
Trial protocol: Outside EU/EEA SK (Completed) PL (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2004-003955-37 | Sponsor Protocol Number: CL3-05590-022 | Start Date*: 2005-03-29 | |||||||||||
Sponsor Name:INSTITUT DE RECHERCHES INTERNATIONALES SERVIER | |||||||||||||
Full Title: Efficacy of perindopril/indapamide combination on coronary Pet Scan parameters. A 6 month, open non controlled stydy in hypertensive patients | |||||||||||||
Medical condition: Essential arterial hypertension | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-003144-23 | Sponsor Protocol Number: PANDA | Start Date*: 2014-02-03 | |||||||||||||||||||||
Sponsor Name:King's College London [...] | |||||||||||||||||||||||
Full Title: Pregnancy And chronic hypertension: NifeDipine or labetalol as Antihypertensive treatment | |||||||||||||||||||||||
Medical condition: Chronic hypertension in pregnancy | |||||||||||||||||||||||
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Population Age: Adults | Gender: Female | ||||||||||||||||||||||
Trial protocol: GB (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2010-021987-13 | Sponsor Protocol Number: NL29900.04 | Start Date*: 2010-10-15 | |||||||||||
Sponsor Name:University Medical Center Groningen | |||||||||||||
Full Title: Renal Hemodynamic Effects of ALiskiren (rasilez) in comparison to ramipril (Tritrace) in patients with overweigHt/obeSiTy and UntreateD hYpertension: The renal HEALTH-STUDY | |||||||||||||
Medical condition: Glomerular hypertension | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-001001-41 | Sponsor Protocol Number: PR002-CLN-pro008 | Start Date*: 2008-06-02 | ||||||||||||||||||||||||||
Sponsor Name:Protherics Medicines Development Ltd, a BTG plc company | ||||||||||||||||||||||||||||
Full Title: A Randomized, Double Blind, Placebo Controlled Study of the Efficacy and Safety of Angiotensin Therapeutic Vaccine (ATV) in Patients With Mild to Moderate Hypertension | ||||||||||||||||||||||||||||
Medical condition: Men and women, 35-70 years old with mild to moderate Hypertension as classified by the British Hypertension Society (BHS) Guidelines - BHS-IV based on the following crietia of sitting blood pressur... | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: GB (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-003567-31 | Sponsor Protocol Number: KPUK0106 | Start Date*: 2007-05-25 | ||||||||||||||||
Sponsor Name:Med. Klinik II, Grosshadern, Klinikum der Universität München | ||||||||||||||||||
Full Title: Regulation of Inflammatory Parameters by Telmisartan in Hypertensive Patients | ||||||||||||||||||
Medical condition: hypertension metabolic syndrome | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Ongoing) | ||||||||||||||||||
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 | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-004853-38 | Sponsor Protocol Number: 111/2006/U/Sper | Start Date*: 2006-11-02 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA DI BOLOGNA POLICLINICO S. ORSOLA M. MALPIGHI | |||||||||||||
Full Title: Effects of Telmisartan on Early Markers of Atherosclerosis in Hypertension with and without Hyperlipidemia | |||||||||||||
Medical condition: hyperlipidemia | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-014542-29 | Sponsor Protocol Number: DYNAMIC-BISOPROLOL-1 | Start Date*: 2009-11-12 | |||||||||||
Sponsor Name:Kari T. Kivistö | |||||||||||||
Full Title: BISOPROLOLIN VAIKUTUS HEMODYNAMIIKKAAN LIEVÄSTI TAI KOHTALAISESTI HYPERTENSIIVISILLÄ MIEHILLÄ: KAKSOISSOKKO, VAIHTOVUOROINEN LUMEKONTROLLOITU TUTKIMUS | |||||||||||||
Medical condition: Lievästi tai kohtalaisesti kohonnut diastolinen verenpaine | |||||||||||||
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Population Age: Adults | Gender: Male | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-004938-16 | Sponsor Protocol Number: 00-MEP-04 | Start Date*: 2008-02-19 | |||||||||||
Sponsor Name:Astellas Pharma Europe B.V. | |||||||||||||
Full Title: A RANDOMISED, DOUBLE-BLIND STUDY TO COMPARE THE EFFECT ON SYMPATHETIC ACTIVITY AND HEMODYNAMIC PROFILE OF BARNIDIPINE AND AMLODIPINE IN PATIENTS WITH MILD TO MODERATE ESSENTIAL HYPERTENSION. | |||||||||||||
Medical condition: Mild to moderate hypertension | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-001131-31 | Sponsor Protocol Number: FHC-1-2012 | Start Date*: 2012-06-14 | |||||||||||
Sponsor Name:Department of Medical Research | |||||||||||||
Full Title: Effekts of nebivolol on the nitric oxide system in patients with essentiel hypertension | |||||||||||||
Medical condition: Essential Hypertension | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-000690-34 | Sponsor Protocol Number: 0954A-327 | Start Date*: 2007-05-29 | |||||||||||
Sponsor Name:Merck Sharp & Dohme OÜ | |||||||||||||
Full Title: A Randomized, Double-Blind, Active Comparator Study to Evaluate the Antihypertensive Efficacy and Safety of Losartan/HCTZ Combination as Compared to Losartan Monotherapy in Pediatric Patients With ... | |||||||||||||
Medical condition: Essential Hypertension | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: EE (Prematurely Ended) FI (Prematurely Ended) LT (Prematurely Ended) HU (Completed) DE (Completed) GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-004235-31 | Sponsor Protocol Number: SEVICONTROL-1 | Start Date*: 2011-12-09 | ||||||||||||||||
Sponsor Name:IPPMed GmbH | ||||||||||||||||||
Full Title: SEVICONTROL-1: Efficacy and safety of a fixed combination of olmesartan 40 mg/amlodipin 10 mg in patients with moderate essential hypertension not sufficiently controlled under monotherapy with can... | ||||||||||||||||||
Medical condition: moderate essential arterial hypertension | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-016738-28 | Sponsor Protocol Number: ALISEI | Start Date*: 2009-12-11 | |||||||||||
Sponsor Name:AZIENDA OSPEDALIERA PISANA | |||||||||||||
Full Title: Phase IV prospective, randomized, open with blind endpoints, parallel group study to evaluate the effect of Aliskiren on endothelial dysfunction in patients with essential hypertension | |||||||||||||
Medical condition: essential hypertension | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-000631-25 | Sponsor Protocol Number: 2007-000631-25 | Start Date*: 2010-06-08 | |||||||||||
Sponsor Name:KAROLINSKA INSTITUTET | |||||||||||||
Full Title: THE ANTITTHROMBOTIC EFFECTS OF DOXAZOSIN AND RAMIPRIL IN ESSENTIAL HYPERTENSION | |||||||||||||
Medical condition: ESSENTIAL HYPERTENSION | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-002422-29 | Sponsor Protocol Number: 1235.8 | Start Date*: 2007-10-19 | |||||||||||
Sponsor Name:Boehringer Ingelheim Ltd. | |||||||||||||
Full Title: An open-label follow-up trial of the efficacy and safety of chronic administration of the combination of telmisartan 40mg + amlodipine 10mg or the combination of telmisartan 80mg + amlodipine 10mg ... | |||||||||||||
Medical condition: essential hypertension | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IE (Completed) GB (Completed) AT (Completed) CZ (Completed) ES (Completed) IT (Completed) BG (Completed) SK (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) |
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