- Trials with a EudraCT protocol (463)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (6)
463 result(s) found for: Antihypertensive.
Displaying page 1 of 24.
EudraCT Number: 2004-004933-32 | Sponsor Protocol Number: km 55/2004 – LORISTAH/CZ | Start Date*: 2005-03-04 |
Sponsor Name:KRKA, d. d., Novo mesto | ||
Full Title: Efficacy and safety of Lorista and Lorista H in the treatment of mild to moderate arterial hypertension | ||
Medical condition: mild to moderate hypertension | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: CZ (Completed) | ||
Trial results: View results |
EudraCT Number: 2018-004809-58 | Sponsor Protocol Number: HEBRO-001 | Start Date*: 2019-04-04 | |||||||||||
Sponsor Name:Institute for study, research, education and therapy of vascular, heart, brain and kidney nosologies (I.N.A.K.E.N) | |||||||||||||
Full Title: Comparative study of eplerenone-based treatment strategy versus irbesartan-based blood pressure lowering in obese hypertensive patients (HEBRO Study) | |||||||||||||
Medical condition: Primary Hypertension and Obesity | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GR (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-006981-40 | Sponsor Protocol Number: hypertension2006-006981-40 | Start Date*: 2007-05-03 | |||||||||||
Sponsor Name:Cambridge University Hospitals NHS Foundation Trust jointly with University of Cambridge | |||||||||||||
Full Title: Does the underlying haemodynamic abnormality determine response to antihypertensive therapy in patients with hypertension? | |||||||||||||
Medical condition: Essential hypertension | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) EE (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-003410-12 | Sponsor Protocol Number: RG_19-169 | Start Date*: 2020-12-16 |
Sponsor Name:University of Birmingham | ||
Full Title: Pregnancy ANtihypertensive Drugs: which Agent is best? | ||
Medical condition: Hypertension in pregnancy (chronic hypertension, gestational hypertension or pre-eclampsia) | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: GB (GB - no longer in EU/EEA) | ||
Trial results: (No results available) |
EudraCT Number: 2004-004231-53 | Sponsor Protocol Number: 506067 | Start Date*: 2004-12-22 |
Sponsor Name:Royal Devon and Exeter NHS Foundation Trust | ||
Full Title: The Effect Of Antihypertensive Treatment With Lisinopril and Labetalol on Baroreflex Sensitivity in Stroke | ||
Medical condition: Stroke | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2011-000538-12 | Sponsor Protocol Number: HLK-VASC-11/01 | Start Date*: 2011-06-14 |
Sponsor Name:VU University Medical Center | ||
Full Title: An exploratory open-label PET-observer-blinded pilot study to evaluate the effect of 3 and 12 months treatment with Aliskeren-based versus amlodipin-based antihypertensive treatment in patients wit... | ||
Medical condition: Abdominal Aortic Aneurysm Hypertension | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2016-002545-32 | Sponsor Protocol Number: CR0002 | Start Date*: 2019-11-06 | |||||||||||
Sponsor Name:Ablative Solutions, Inc | |||||||||||||
Full Title: A Pivotal, Multicenter, Blinded, Sham Procedure-Controlled Trial of Renal Denervation by the Peregrine System™ Kit, in Subjects with Hypertension. | |||||||||||||
Medical condition: Hypertension | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) FR (Trial now transitioned) SE (Ongoing) BE (Trial now transitioned) NL (Trial now transitioned) IE (Trial now transitioned) PL (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2004-002232-26 | Sponsor Protocol Number: LERCA-GLOMERULAR | Start Date*: 2004-11-04 |
Sponsor Name:HOSPITAL 12 OCTUBRE | ||
Full Title: CHANGES IN GLOMERULAR HEMODINAMICS PARAMETERS IN HIPERTENSIVE PATIENTS AFTER TREATMENT WITH LERCANIDIPINE | ||
Medical condition: HYPERTENSION | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2006-004846-17 | Sponsor Protocol Number: STH 14399 | Start Date*: 2007-03-16 | |||||||||||
Sponsor Name:Sheffield Teaching Hospitals NHS Foundation Trust | |||||||||||||
Full Title: A randomised, placebo controlled trial of the efficacy of the addition of spironolactone to modern antihypertensive treatment regimes in patients with resistant hypertension. | |||||||||||||
Medical condition: Resistant hypertension. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2021-001404-14 | Sponsor Protocol Number: QGC001-3QG2 | Start Date*: 2021-08-17 | |||||||||||
Sponsor Name:Quantum Genomics | |||||||||||||
Full Title: A Phase 3, Double-blind, Placebo-controlled and Open-label Efficacy and Long-term Safety Study of Firibastat (QGC001) Administered Orally, Once Daily, for Up to 48 Weeks in Patients with Difficult-... | |||||||||||||
Medical condition: Treatment of patients with difficult-to-treat and/or treatment-resistant hypertension (HTN) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SK (Prematurely Ended) HU (Prematurely Ended) ES (Ongoing) CZ (Prematurely Ended) IT (Completed) NL (Prematurely Ended) BE (Completed) BG (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-003535-20 | Sponsor Protocol Number: CS8635-A-E303 | Start Date*: 2009-04-07 | |||||||||||
Sponsor Name:DAIICHI SANKYO EUROPE GmbH | |||||||||||||
Full Title: A RANDOMISED, DOUBLE-BLIND, ADD-ON STUDY OF HYDROCHLOROTHIAZIDE IN SUBJECTS WITH MODERATE TO SEVERE HYPERTENSION NOT ACHIEVING TARGET BLOOD PRESSURE ON OLMESARTAN MEDOXOMIL/AMLODIPINE FIXED DOSE CO... | |||||||||||||
Medical condition: Essential hypertension | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) NL (Completed) FR (Completed) BE (Completed) ES (Completed) AT (Completed) CZ (Completed) DK (Completed) SK (Completed) BG (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-004509-29 | Sponsor Protocol Number: QGC001-3QG1 | Start Date*: 2020-04-27 |
Sponsor Name:Quantum Genomics | ||
Full Title: A Phase 3, Double-blind, Placebo-controlled, Efficacy and Safety Study of Firibastat (QGC001) Administered Orally, Twice Daily, Over 12 Weeks in Difficult-to-treat/Resistant Hypertensive Subjects | ||
Medical condition: Treatment of hypertension (HTN) in difficult-to-treat and/or treatment resistant patients | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Completed) DE (Completed) PL (Completed) ES (Ongoing) CZ (Completed) HU (Completed) BG (Completed) | ||
Trial results: View results |
EudraCT Number: 2018-000036-96 | Sponsor Protocol Number: CR0014 | Start Date*: 2018-09-06 | |||||||||||
Sponsor Name:Ablative Solutions, Inc. | |||||||||||||
Full Title: A Phase 2, Multicenter, Blinded, Sham Procedure-Controlled Trial of Renal Denervation by the Peregrine System Kit, in Subjects with Hypertension, in the Absence of Antihypertensive Medications | |||||||||||||
Medical condition: Hypertension | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: BE (Completed) GB (GB - no longer in EU/EEA) DE (Completed) IE (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2004-000020-32 | Sponsor Protocol Number: CV131-176 | Start Date*: 2005-02-16 |
Sponsor Name:Bristol Myers Squibb International Corporation | ||
Full Title: The Efficacy and Safety of Irbesartan/HCTZ Combination Therapy as First Line Treatment for Severe Hypertension | ||
Medical condition: Severe Hypertension | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2005-003182-16 | Sponsor Protocol Number: A07329 | Start Date*: 2005-08-26 |
Sponsor Name:Addenbrooke's Hospital Trust | ||
Full Title: Blood Pressure Optimisation In Patients With Polycystic Kidney Disease And Hypertension By Rotation Through The Main Therapeutic Classes Of Antihypertensive Drugs. | ||
Medical condition: Polycystic kidney disease | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2011-005344-95 | Sponsor Protocol Number: 3004 | Start Date*: 2012-06-15 |
Sponsor Name:Steno Diabetes Center | ||
Full Title: Time course of the blood pressure lowering effect of liraglutide therapy in type 2 diabetes | ||
Medical condition: type 2 diabetes | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DK (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2015-000577-13 | Sponsor Protocol Number: kajakbe191086 | Start Date*: 2015-09-09 |
Sponsor Name:Oslo University Hospital | ||
Full Title: Therapeutic effects of BNP in uncontrolled hypertensive patients 1 | ||
Medical condition: Uncontrolled hypertension (UHT, i.e. blood pressure ≥ 150/90, or ≥ 150/85 mm Hg in diabetic patients) despite treatment with at least two different classes of antihypertensive medications. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NO (Prematurely Ended) | ||
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: 2004-001061-17 | Sponsor Protocol Number: CSPP100A2306 | Start Date*: 2005-04-12 |
Sponsor Name:Novartis Pharma Services AG | ||
Full Title: A 26 week, double-blind, randomized, multicenter, parallel group, active-controlled study comparing aliskiren to ramipril with optional addition of hydrochlorothiazide (HCTZ), followed by a 4 week ... | ||
Medical condition: Hypertension | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SK (Completed) DK (Completed) IS (Completed) BE (Completed) ES (Completed) | ||
Trial results: View results |
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) |
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