- Trials with a EudraCT protocol (224)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
224 result(s) found for: Ambulatory blood pressure.
Displaying page 1 of 12.
EudraCT Number: 2012-000509-54 | Sponsor Protocol Number: MB121-008 | Start Date*: 2012-09-12 | |||||||||||
Sponsor Name:Bristol-Myers Squibb International Corporation | |||||||||||||
Full Title: A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel Group, Phase 2B Trial to Evaluate the Safety and Efficacy of BMS-823778 in Overweight and Obese Subjects with Inadequately Cont... | |||||||||||||
Medical condition: Hypertension | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Completed) HU (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: 2008-000869-38 | Sponsor Protocol Number: VGSKAS-12916 | Start Date*: 2008-06-02 |
Sponsor Name:Skaraborg Hospital | ||
Full Title: Impact of Losartan in hypertensive men with obstructive sleep apnea | ||
Medical condition: Hypertension and obstructive sleep apnea (OSA) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2012-001066-14 | Sponsor Protocol Number: DENERVHTA | Start Date*: 2012-07-17 |
Sponsor Name:Consorci Mar Parc de salut de Barcelona ( Parc de Salut Mar) | ||
Full Title: Sympathetic renal denervation versus increment of pharmacological treatment in resistant arterial hypertension | ||
Medical condition: subjects with resistant hypertension | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
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: 2009-018125-70 | Sponsor Protocol Number: ENM-EA-016 | Start Date*: 2011-04-06 |
Sponsor Name:Medizinische Universität Graz | ||
Full Title: Styrian Vitamin D Hypertension Trial: A randomized, double-blind, placebo controlled trial to study the effects of vitamin D supplementation on systolic blood pressure in vitamin D deficient hypert... | ||
Medical condition: Patients with arterial hypertension and vitamin D deficiency | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Completed) | ||
Trial results: View results |
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: 2020-004891-16 | Sponsor Protocol Number: CL3-05179-002 | Start Date*: 2021-10-20 | |||||||||||
Sponsor Name:Institut de Recherches Internationales Servier | |||||||||||||
Full Title: Evaluation of the clinical efficacy and safety of perindopril 10 mg/indapamide 2.5 mg/amlodipine 5 or 10 mg/bisoprolol 5 mg in single-pill combination after 8 weeks of treatment versus the free com... | |||||||||||||
Medical condition: Hypertension | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: PL (Completed) PT (Completed) LT (Completed) IT (Completed) LV (Completed) SK (Completed) HU (Completed) CZ (Completed) BG (Completed) HR (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2017-000213-23 | Sponsor Protocol Number: NL60561.078.17 | Start Date*: 2017-07-21 |
Sponsor Name: | ||
Full Title: ARNI-study: ARNI or ARB to arrest progression of nephropathy. | ||
Medical condition: Chronic kidney disease with concurrent hypertension and diabetes. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2013-003204-40 | Sponsor Protocol Number: PATHBP_2013 | Start Date*: 2014-01-20 | ||||||||||||||||||||||||||||||||||||||||||||||
Sponsor Name:University of Edinburgh [...] | ||||||||||||||||||||||||||||||||||||||||||||||||
Full Title: Paracetamol treatment in hypertension: effect on blood pressure | ||||||||||||||||||||||||||||||||||||||||||||||||
Medical condition: Hypertension | ||||||||||||||||||||||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||||||||||||
Trial protocol: GB (Completed) | ||||||||||||||||||||||||||||||||||||||||||||||||
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: 2013-001643-30 | Sponsor Protocol Number: CLCZ696A2320 | Start Date*: 2013-10-09 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: An 8-week randomized, double-blind, placebo-controlled factorial study to evaluate the efficacy and safety of LCZ696 alone and in combination with amlodipine in patients with essential hypertension | |||||||||||||
Medical condition: Essential hypertension | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SK (Completed) ES (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: 2004-004255-18 | Sponsor Protocol Number: CSPP100A2324 | Start Date*: 2005-03-30 |
Sponsor Name:Novartis Pharma Services AG | ||
Full Title: An 8-week, randomized, double-blind, parallel-group, multicenter study assessing the efficacy and safety of aliskiren 75 mg, 150 mg, and 300 mg in patients ≥ 65 years of age with essential hyperten... | ||
Medical condition: Hypertension | ||
Disease: | ||
Population Age: Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) AT (Completed) IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2004-004865-14 | Sponsor Protocol Number: CVAL489ADE19 | Start Date*: 2005-04-06 | |||||||||||
Sponsor Name:Novartis Pharma GmbH | |||||||||||||
Full Title: A 2 x 5 weeks open label, multicenter, randomized cross-over study to compare the reduction of predialysis systolic blood pressure with valsartan (Diovan) 80 mg compared to irbesartan150 mg in pati... | |||||||||||||
Medical condition: Hypertension | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2008-001305-42 | Sponsor Protocol Number: CSPP100A2405 | Start Date*: 2008-05-29 |
Sponsor Name:Novartis Pharma Services AG | ||
Full Title: An eight-week double-blind, multi-center, randomized, placebo-controlled, parallel-group study to evaluate the efficacy and safety of aliskiren 75mg, 150mg and 300mg in elderly patients with essent... | ||
Medical condition: hypertension | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SK (Completed) IS (Completed) FR (Completed) NL (Completed) CZ (Completed) IT (Completed) | ||
Trial results: View results |
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: 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: 2014-003737-26 | Sponsor Protocol Number: A3191342 | Start Date*: 2015-04-07 |
Sponsor Name:Pfizer Inc | ||
Full Title: A Phase 4, 6-week, randomized double-blind, multicenter, active-controlled trial to evaluate the effects of Celecoxib (Celebrex®) or Naproxen on blood pressure in paediatric subjects with juvenile ... | ||
Medical condition: Juvenile idiopathic arthritis | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: Outside EU/EEA | ||
Trial results: View results |
EudraCT Number: 2015-003049-24 | Sponsor Protocol Number: PHY201501 | Start Date*: 2016-07-27 |
Sponsor Name:Uppsala University, Department of Medical Sciences | ||
Full Title: The Precision Hypertension Care study | ||
Medical condition: Hypertension | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: View results |
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