- Trials with a EudraCT protocol (501)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
501 result(s) found for: Systolic hypertension.
Displaying page 1 of 26.
EudraCT Number: 2008-004534-24 | Sponsor Protocol Number: 2007CV09 | Start Date*: 2008-11-18 | |||||||||||
Sponsor Name:University of Dundee | |||||||||||||
Full Title: Can high-dose vitamin D supplementation reduce blood pressure and markers of cardiovascular risk in older people with isolated systolic hypertension? | |||||||||||||
Medical condition: Isolated systolic hypertension | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
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: 2013-001227-40 | Sponsor Protocol Number: SMR-2271(SER100-001) | Start Date*: 2013-09-23 | |||||||||||
Sponsor Name:Serodus ASA | |||||||||||||
Full Title: A randomized, double-blind, placebo-controlled, cross-over, multi-center study assessing the safety, tolerability and efficacy of SER100 10 mg s.c. twice daily for 2 days in patients with Isolated ... | |||||||||||||
Medical condition: Isolated Systolic Hypertension | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NO (Completed) FI (Prematurely Ended) HU (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
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: 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: 2006-004224-37 | Sponsor Protocol Number: EREMIT | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Universität Leipzig | |||||||||||||
Full Title: Everolimus in der Therapie von Patienten mit pulmonaler Hypertonie | |||||||||||||
Medical condition: - steady or progressive pulmonary hypertension accompanied by at least two of the following parameters associated with a poor prognosis: - Cardiac index ≤ 2,1 l/min/m2 - 6 MWD ≤ 380 m - systolic RR... | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
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: 2022-001283-10 | Sponsor Protocol Number: NL80929.091.22 | Start Date*: 2022-06-28 |
Sponsor Name:Radboud University Medical Center | ||
Full Title: The effects of medication induced blood pressure reduction on cerebral hemodynamics in hypertensive frail elderly | ||
Medical condition: Hypertension | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: NL (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: 2013-001783-36 | Sponsor Protocol Number: CLCZ696A2318 | Start Date*: 2013-08-27 | |||||||||||
Sponsor Name:Novartis Farmacéutica, S.A. | |||||||||||||
Full Title: A randomized 8-week double-blind, parallel-group, active-controlled, multicenter study to evaluate efficacy and safety of LCZ696 200 mg in comparison with olmesartan 20 mg in essential hypertensive... | |||||||||||||
Medical condition: Hypertension | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-003459-76 | Sponsor Protocol Number: 09F401 | Start Date*: 2015-02-03 | |||||||||||
Sponsor Name:Istituto Auxologico Italiano, IRCCS | |||||||||||||
Full Title: REducing blood pressure Variability in Essential hypertension with RAmipril vErsus Nifedipine GITS Trial | |||||||||||||
Medical condition: essential hypertension | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) GR (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: 2009-011296-80 | Sponsor Protocol Number: CSPP100AFR01 | Start Date*: 2009-06-10 | |||||||||||
Sponsor Name:Novartis Pharma S.A.S | |||||||||||||
Full Title: Efficacy of Rasilez® (Aliskiren) compared to ramipril in the treatment of moderate systolic hypertensive patients | |||||||||||||
Medical condition: Hypertension artérielle systolique | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-003071-37 | Sponsor Protocol Number: QGC001/2QG1 | Start Date*: 2014-11-14 | |||||||||||
Sponsor Name:Quantum Genomics | |||||||||||||
Full Title: Multicenter, randomized, double-blind, two-period, placebo controlled, forced-titration proof of concept crossover study to compare QGC001 with placebo in patients with grade I or II essential hype... | |||||||||||||
Medical condition: Hyperactivity of the brain renin-angiotensin system participates to the development and maintenance of essential Hypertension | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (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: 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: 2020-001014-37 | Sponsor Protocol Number: ALTUM | Start Date*: 2020-08-13 | ||||||||||||||||
Sponsor Name:OSPEDALE SAN RAFFAELE | ||||||||||||||||||
Full Title: Pharmacogenetics of hypertension: randomized monocentric study in patients with essential hypertension and treated with Spironolactone or Torasemide | ||||||||||||||||||
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: 2006-001823-20 | Sponsor Protocol Number: CMA-0601-PR-0004 | Start Date*: 2006-06-22 | |||||||||||
Sponsor Name:CHIESI | |||||||||||||
Full Title: A twelve-week, multicentre, double blind, randomised, parallel group, clinical study to assess the antihypertensive efficacy of delapril 15 mg b.i.d. and 30 mg b.i.d. versus lisinopril and placebo | |||||||||||||
Medical condition: hypertension | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
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: 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 |
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