- Trials with a EudraCT protocol (104)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
104 result(s) found for: Antihypertensive drugs.
Displaying page 1 of 6.
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: 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: 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: 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: 2006-001898-25 | Sponsor Protocol Number: DAR-311 | Start Date*: 2006-09-21 | |||||||||||
Sponsor Name:Gilead Sciences, Inc. | |||||||||||||
Full Title: DORADO - Fixed Doses of Darusentan as Compared to Placebo in Resistant Hypertension A Phase 3 Randomized, Double-Blind, Placebo-Controlled, Multi-Center, Parallel Group Study to Evaluate the Effica... | |||||||||||||
Medical condition: Resistant hypertension | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) DK (Completed) DE (Completed) GB (Completed) ES (Completed) IT (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: 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: 2006-006861-18 | Sponsor Protocol Number: 20061212 | Start Date*: 2007-03-26 |
Sponsor Name:Department of Cardiology | ||
Full Title: Comparison between beta-adrenergic blockers and angiotensin II receptor antagonists for the treatment of late hypertension in patients with repaired aortic coarctation | ||
Medical condition: Aortic coarctation and late hypertension | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2014-000605-12 | Sponsor Protocol Number: notapplicable1 | Start Date*: 2014-06-13 |
Sponsor Name: | ||
Full Title: Thiazide diuretics versus calcium channel blockers for the treatment of calcineurin inhibitor-induced hypertension in patients with psoriasis or eczema: a single-center randomized cross-over trial. | ||
Medical condition: Hypertension, induced by the use of a Calcineurin Inhibitor (CNI) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2012-004704-35 | Sponsor Protocol Number: NL39417.078.12 | Start Date*: 2012-11-22 |
Sponsor Name: | ||
Full Title: Thiazide diuretics versus calcium channel blockers for the treatment of tacrolimus-induced hypertension in dermatology patients: a single-center randomized cross-over trial. | ||
Medical condition: Hypertension, induced by the use of a Calcineurin Inhibitor (CNI) | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2005-001214-40 | Sponsor Protocol Number: cro085 | Start Date*: 2007-08-17 |
Sponsor Name:Imperial College London | ||
Full Title: A trial to compare the effects of nebivolol versus atenolol on various cardiovascular measurements including insulin sensitivity | ||
Medical condition: Hypertension | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2016-000165-23 | Sponsor Protocol Number: INFORM | Start Date*: 2016-10-19 | |||||||||||
Sponsor Name:Cambridge University Hospitals NHS Foundation Trust and University of Cambridge | |||||||||||||
Full Title: ComparIsoN oF Optimal Hypertension RegiMens (Part of the Ancestry Informative Markers in Hypertension (AIM HY) Programme – AIM HY-INFORM) | |||||||||||||
Medical condition: Cardiovascular Hemodynamics | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-003547-23 | Sponsor Protocol Number: DAR-312 | Start Date*: 2007-11-15 | |||||||||||
Sponsor Name:Gilead Sciences, Inc. | |||||||||||||
Full Title: DORADO-AC - Optimized Doses of Darusentan as Compared to an Active Control in Resistant Hypertension A Phase 3 Randomized, Double-Blind, Placebo- and Active-Controlled, Multi-center, Parallel Grou... | |||||||||||||
Medical condition: Resistant hypertension | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Completed) GB (Completed) DE (Completed) BE (Completed) DK (Completed) ES (Completed) CZ (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-002008-41 | Sponsor Protocol Number: GR-MET-19 | Start Date*: 2019-09-05 | |||||||||||
Sponsor Name:AOU DI BOLOGNA POLICLINICO S.ORSOLA-MALPIGHI | |||||||||||||
Full Title: Effect of metyrapone on cardiovascular risk factors in patients with adrenal incidentalomas and subclinical/mild Cushing's syndrome | |||||||||||||
Medical condition: patients with adrenal incidentalomas and subclinical/mild Cushing’s syndrome | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2014-002544-40 | Sponsor Protocol Number: 5866 | Start Date*: 2014-10-29 |
Sponsor Name:Hôpitaux Universitaires de Strasbourg | ||
Full Title: THE TREATMENT OF HYPERTENSION ASSOCIATED WITH SEVERE PREECLAMPSIA. A RANDOMIZED CONTROLLED TRIAL OF URAPIDIL VERSUS NICARDIPINE. The URANIC trial. | ||
Medical condition: Hypertension associated with severe pre eclampsia | ||
Disease: | ||
Population Age: Adults | Gender: Female | |
Trial protocol: FR (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2020-003647-28 | Sponsor Protocol Number: NA | Start Date*: 2020-12-09 |
Sponsor Name: | ||
Full Title: Differences in antihypertensive drug levels in patients with hypertension: old vs young 2 | ||
Medical condition: Hypertension Cardiovascular disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2010-021988-32 | Sponsor Protocol Number: LUMI/10/ZOF- HYP/001 | Start Date*: 2010-09-27 | |||||||||||
Sponsor Name:LUSOFARMACO | |||||||||||||
Full Title: A multicentre, multinational, randomised, double-blind, pilot, ascending dose for non responder, parallel group study on the therapeutic efficacy and safety of o.d. Zofenopril 30 mg plus HCTZ 12.5 ... | |||||||||||||
Medical condition: elderly subjects (age > 65 years) affected by Isolated Systolic Hypertension | |||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2009-015824-27 | Sponsor Protocol Number: MeBN/06/NEB-CBP/001 | Start Date*: 2009-12-23 |
Sponsor Name:MENARINI Benelux NV/SA | ||
Full Title: The effects of Nebivolol/HCTZ on Central Arterial Pressure, a randomised double-blind cross-over trial | ||
Medical condition: Hypertension | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-000628-25 | Sponsor Protocol Number: 23012008 | Start Date*: 2008-05-13 |
Sponsor Name:UMC Utrecht | ||
Full Title: The effectiveness of intensive treatment on sympathetic hyperactivity. A randomized, cross-over trial in patients with chronic kidney disease and hypertension | ||
Medical condition: Sympathetic nerve system in hypertensive patients with chronic kidney disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
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) |
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