- Trials with a EudraCT protocol (93)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
93 result(s) found for: Resistant Hypertension.
Displaying page 1 of 5.
EudraCT Number: 2019-002334-36 | Sponsor Protocol Number: 2018/350/HP | Start Date*: 2021-12-02 | |||||||||||||||||||||
Sponsor Name:CHU de Rouen | |||||||||||||||||||||||
Full Title: VASCULAR AND RENAL IMPACT OF ENDOTHELIN-1 RECEPTOR BLOCKADE IN PATIENTS WITH RESISTANT ARTERIAL HYPERTENSION | |||||||||||||||||||||||
Medical condition: Resistant arterial hypertension | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: FR (Trial now transitioned) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2015-001890-42 | Sponsor Protocol Number: CLHW090X2202 | Start Date*: 2016-04-04 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A randomized, sponsor open, site and subject double-blind, parallel group, placebo-controlled study to evaluate the safety and efficacy of LHW090 after 4 weeks treatment in patients with resistant ... | |||||||||||||
Medical condition: Resistant hypertension | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) FR (Completed) DK (Completed) NL (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-002681-63 | Sponsor Protocol Number: 2007CV04 | Start Date*: 2008-08-28 | |||||||||||
Sponsor Name:Research and Innovation Services, University of Dundee | |||||||||||||
Full Title: DOES VITAMIN D REDUCE BLOOD PRESSURE AND LV MASS IN RESISTANT HYPERTENSIVE PATIENTS WITH VITAMIN D INSUFFICIENCY? | |||||||||||||
Medical condition: Resistant Hypertension | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-001998-25 | Sponsor Protocol Number: BLO K025 | Start Date*: 2006-09-29 | |||||||||||
Sponsor Name:Takeda Pharma GmbH | |||||||||||||
Full Title: Double-blind, randomised trial to investigate the antihypertensive and metabolic effects of candesartan in insulin-resistant obese patients with a hypertension not adequately controlled by previous... | |||||||||||||
Medical condition: Insulin-resistant obese patients with a hypertension not adequately controlled by previous beta-blocker or calcium channel blocker | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
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: 2007-003558-27 | Sponsor Protocol Number: ASPIRANT | Start Date*: 2007-07-30 | |||||||||||||||||||||
Sponsor Name:Olomouc University Hospital and Palacký University School of Medicine, Internal Medicine Dept. I | |||||||||||||||||||||||
Full Title: Addition of spironolactone in patients with resistant arterial hypertension (ASPIRANT) | |||||||||||||||||||||||
Medical condition: arterial hypertension resistant to treatment (target blood pressure not reached with a combination of at least three different antihypertensive drugs, one of them being a diuretic) | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: CZ (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-007338-23 | Sponsor Protocol Number: CLCI699A2216 | Start Date*: 2009-02-18 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A phase II, randomized, double-blind, placebo and active controlled, parallel group, multi-center, dose ranging study to evaluate the efficacy and safety of LCI699 compared to placebo after 8 weeks... | |||||||||||||
Medical condition: resistant hypertension | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IS (Completed) | |||||||||||||
Trial results: View results |
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: 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 | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-004995-13 | Sponsor Protocol Number: 38372 | Start Date*: 2012-02-09 | |||||||||||
Sponsor Name:Erasmus MC | |||||||||||||
Full Title: Endovascular renal sympathetic denervation versus spironolactone for treatment-resistant hypertension: a randomized, multicentric study | |||||||||||||
Medical condition: Hypertension | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-001004-39 | Sponsor Protocol Number: JO-3 | Start Date*: 2005-07-05 |
Sponsor Name:University of Edinburgh | ||
Full Title: Investigation of combined phosphodiesterase 5 inhibitor and isosorbide mononitrate for the treatment of resistant hypertension | ||
Medical condition: Hypertension | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
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: 2008-000874-19 | Sponsor Protocol Number: 1235.21 | Start Date*: 2008-11-19 | ||||||||||||||||
Sponsor Name:Boehringer Ingelheim Pharmaceuticals. Inc. | ||||||||||||||||||
Full Title: A Phase III, eight week randomised double-blind, double-dummy, forced titration study to compare the fixed-dose combination tablet of telmisartan 80 mg plus amlodipine 10 mg versus amlodipine 10 mg... | ||||||||||||||||||
Medical condition: type 2 diabetes and mild to moderate hypertension | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Completed) ES (Completed) SK (Completed) SE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2011-000785-35 | Sponsor Protocol Number: PAIR | Start Date*: 2011-04-13 | ||||||||||||||||
Sponsor Name:IST. DI RICERCHE FARMACOLOG. M. NEGRI | ||||||||||||||||||
Full Title: A PROSPECTIVE STUDY TO ASSESS THE INTERACTION BETWEEN PATIENT GENOTYPE AND ROSTAFUROXIN EFFECTS ON ARTERIAL BLOOD PRESSURE AND KIDNEY FUNCTION IN NEVER-TREATED HYPERTENSIVE TYPE 2 DIABETES PATIENT... | ||||||||||||||||||
Medical condition: Type 2 Diabetes. | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-001899-20 | Sponsor Protocol Number: DAR-311-E | Start Date*: 2007-01-16 | |||||||||||
Sponsor Name:Gilead Sciences Inc. | |||||||||||||
Full Title: DORADO-EX – A Dose-Blinded, Long-Term Safety Extension Study to the Phase 3 DORADO Study (Protocol DAR-311) of Darusentan in Resistant Hypertension A Dose-Blinded, Long-Term Safety Extension Study... | |||||||||||||
Medical condition: Resistant hypertension | |||||||||||||
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Population Age: | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) DK (Completed) SE (Prematurely Ended) FR (Completed) DE (Prematurely Ended) IT (Prematurely Ended) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-006436-22 | Sponsor Protocol Number: BAY a 1040 - BAY 68-9291/12313 | Start Date*: 2007-08-29 | |||||||||||
Sponsor Name:BAYER | |||||||||||||
Full Title: A multicenter Study Evaluating the Efficacy of Nifedipine GITS ヨ Telmisartan Combination in Blood Pressure Control and Beyond: comparison of two strategies. | |||||||||||||
Medical condition: Hypertension | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-002657-38 | Sponsor Protocol Number: RLY5016-207 | Start Date*: 2017-01-09 | ||||||||||||||||
Sponsor Name:Relypsa, Inc | ||||||||||||||||||
Full Title: A Randomized, Double-Blind, Placebo controlled, Parallel Group Study of Patiromer for the Enablement of Spironolactone Use for Blood Pressure Control in Patients with Resistant Hypertension and Chr... | ||||||||||||||||||
Medical condition: Resistant Hypertension and Chronic Kidney Disease | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: HU (Completed) DE (Completed) HR (Completed) BG (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-007749-29 | Sponsor Protocol Number: UKCRN4499 | Start Date*: 2009-09-02 | |||||||||||
Sponsor Name:R&D Department, [...] | |||||||||||||
Full Title: Monotherapy vs Dual Therapy for Initial Treatment for hypertension | |||||||||||||
Medical condition: Resistant Hypertension | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-003548-42 | Sponsor Protocol Number: DAR-312-E | Start Date*: 2008-04-15 | |||||||||||
Sponsor Name:Gilead Sciences, Inc. | |||||||||||||
Full Title: DORADO-AC-EX – A Double-Blind, Active-Controlled, Long-Term Safety Extension Study to the Phase 3 DORADO-AC Study (Protocol DAR-312) of Darusentan in Resistant Hypertension A Double-Blind, Active-... | |||||||||||||
Medical condition: Resistant hypertension | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) DK (Prematurely Ended) BE (Completed) FR (Completed) DE (Prematurely Ended) ES (Completed) CZ (Prematurely Ended) | |||||||||||||
Trial results: View results |
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 |
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