- Trials with a EudraCT protocol (690)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (2)
690 result(s) found for: Arterial Hypertension.
Displaying page 13 of 35.
EudraCT Number: 2010-019883-36 | Sponsor Protocol Number: CAMN107X2201 | Start Date*: 2010-08-31 | |||||||||||
Sponsor Name:Novartis Pharma AG | |||||||||||||
Full Title: A 24 week, randomized, double blind, multicenter, placebo-controlled efficacy, safety, tolerability and PK trial of Nilotinib (Tasigna®, AMN107) in Pulmonary Arterial Hypertension (PAH) | |||||||||||||
Medical condition: Pulmonary Arterial Hypertension (PAH) Class II or III patients remaining symptomatic despite at least one PAH-specific therapy. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Prematurely Ended) IT (Prematurely Ended) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-000165-12 | Sponsor Protocol Number: RLY5016-205 | Start Date*: 2011-05-27 | |||||||||||||||||||||
Sponsor Name:Relypsa, Inc. | |||||||||||||||||||||||
Full Title: A Multicenter, Randomized, Open-Label, Dose Ranging Study to Evaluate the Efficacy and Safety of RLY5016 in the Treatment of Hyperkalemia in Patients with Hypertension and Diabetic Nephropathy Rece... | |||||||||||||||||||||||
Medical condition: Hyperkalemia in Patients with Hypertension and Diabetic Nephropathy | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: HU (Completed) DE (Prematurely Ended) AT (Prematurely Ended) SI (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-000645-23 | Sponsor Protocol Number: Borealis1 | Start Date*: 2015-06-19 | ||||||||||||||||
Sponsor Name:CIBER (Centro de Investigacion Biomedica en Red) | ||||||||||||||||||
Full Title: Safety, tolerability and efficacy of nocturnal hypertension treatment with domperidone in the sleep apnea-hypopnea syndrome. Pilot study. | ||||||||||||||||||
Medical condition: Nocturnal hypertension in the sleep apnea-hypopnea syndrome. | ||||||||||||||||||
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Population Age: Adults | Gender: Male | |||||||||||||||||
Trial protocol: ES (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2008-005886-78 | Sponsor Protocol Number: B1321002 | Start Date*: 2010-01-12 | |||||||||||
Sponsor Name:Pfizer Ltd. | |||||||||||||
Full Title: A PHASE 3, MULTI-CENTER, OPEN LABEL STUDY TO EVALUATE THE LONG-TERM SAFETY OF MONOTHERAPY SITAXSENTAN SODIUM AND COMBINATION THERAPY WITH SITAXSENTAN SODIUM AND SILDENAFIL CITRATE IN SUBJECTS WITH ... | |||||||||||||
Medical condition: PULMONARY ARTERIAL HYPERTENSION | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Prematurely Ended) SK (Prematurely Ended) BG (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-003042-27 | Sponsor Protocol Number: APD811-007 | Start Date*: 2015-04-23 | |||||||||||
Sponsor Name:United Therapeutics Corporation | |||||||||||||
Full Title: An Open-Label Extension Study of APD811-003 in Patients with Pulmonary Arterial Hypertension | |||||||||||||
Medical condition: Pulmonary Arterial Hypertension | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: CZ (Completed) HU (Completed) ES (Ongoing) PL (Completed) RO (Ongoing) SK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2005-001967-70 | Sponsor Protocol Number: AC-052-367 | Start Date*: 2005-10-13 |
Sponsor Name:Actelion Pharmaceuticals Ltd. | ||
Full Title: An open-label, long-term, safety, and tolerability extension study using the pediatric formulation of bosentan in the treatment of children with idiopathic or familial pulmonary arterial hypertensi... | ||
Medical condition: Idiopathic or familial pulmonary arterial hypertension | ||
Disease: | ||
Population Age: Children, Under 18 | Gender: Male, Female | |
Trial protocol: GB (Completed) DE (Completed) IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-002314-21 | Sponsor Protocol Number: MEN IFR/08/NEB-HYP/01 | Start Date*: 2008-05-23 | ||||||||||||||||
Sponsor Name:A. MENARINI I.F.R. | ||||||||||||||||||
Full Title: VALUTAZIONE COMPARATIVA DEGLI EFFETTI SULLA FUNZIONE ENDOTELIALE DEL TRATTAMENTO CON NEBIVOLOLO E IDROCLOROTIAZIDE VS IRBESARTAN E IDROCLOROTIAZIDE IN PAZIENTI CON IPERTENSIONE ARTERIOSA NEO-DIAGNO... | ||||||||||||||||||
Medical condition: IPERTENSIONE ARTERIOSA | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: IT (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2004-005157-63 | Sponsor Protocol Number: AC-052-365 | Start Date*: 2005-06-15 |
Sponsor Name:Actelion Pharmaceuticals Ltd. | ||
Full Title: An open label, multicenter study to assess the pharmacokinetics, tolerability, and safety of a pediatric formulation of bosentan in children with idiopathic or familial pulmonary arterial hypertens... | ||
Medical condition: Idiopathic or familial PAH | ||
Disease: | ||
Population Age: Children, Under 18 | Gender: Male, Female | |
Trial protocol: GB (Completed) IT (Completed) | ||
Trial results: View results |
EudraCT Number: 2007-002469-11 | Sponsor Protocol Number: CSPP100A2403 | Start Date*: 2008-05-13 | |||||||||||
Sponsor Name:Novartis Farmaceutica S.A. | |||||||||||||
Full Title: Estudio aleatorizado, doble ciego, de grupos paralelos, multicéntrico, para comparar la eficacia y seguridad de aliskiren 300 mg administrado una vez al día y de aliskiren 150 mg administrado dos v... | |||||||||||||
Medical condition: Hipertension | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-003921-13 | Sponsor Protocol Number: 12/0368 | Start Date*: 2013-06-07 | |||||||||||
Sponsor Name:University College London | |||||||||||||
Full Title: COMbination therapy for PulmonAry hypertension using RacEcadotril (COMPARE). | |||||||||||||
Medical condition: Pulmonary hypertension | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2011-004631-31 | Sponsor Protocol Number: REM-PH-416 | Start Date*: 2012-03-13 | |||||||||||||||||||||
Sponsor Name:United Therapeutics Corp. | |||||||||||||||||||||||
Full Title: A 16 Week, Open Label, Multi-Centre, Study to Evaluate the Safety, Tolerability and Pharmacodynamic Effects of a Rapid Dose Titration Regimen of Subcutaneous Remodulin® Therapy in Subjects with Pul... | |||||||||||||||||||||||
Medical condition: Pulmonary Arterial Hypertension (PAH) | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: DE (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2022-001900-17 | Sponsor Protocol Number: 2020/0431/HP | Start Date*: 2022-10-24 | |||||||||||
Sponsor Name:DRCI - CHU de Rouen | |||||||||||||
Full Title: PILOT STUDY OF THE EFFECT OF A SUBSTANCE P ANTAGONIST, APREPITANT, ON THE SECRETION OF ALDOSTERONE IN PATIENTS WITH OBSTRUCTIVE SLEEP APNEA AND ARTERIAL HYPERTENSION SYNDROME | |||||||||||||
Medical condition: Patients with obstructive sleep apnea syndrome with 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: 2009-010170-38 | Sponsor Protocol Number: CSPP100G2301 | Start Date*: 2010-07-21 | ||||||||||||||||
Sponsor Name:Novartis Pharma Services AG | ||||||||||||||||||
Full Title: A Randomized Controlled Trial of Aliskiren in the Prevention of Major Cardiovascular Events in Elderly People Aliskiren Prevention Of Later Life Outcomes (APOLLO) | ||||||||||||||||||
Medical condition: cardiovacular disease, fonctional hypertension, | ||||||||||||||||||
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Population Age: Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: SE (Prematurely Ended) HU (Completed) DE (Completed) IE (Prematurely Ended) CZ (Prematurely Ended) ES (Prematurely Ended) NL (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2013-002348-99 | Sponsor Protocol Number: AUTH88622 | Start Date*: 2014-09-22 | ||||||||||||||||
Sponsor Name:Aristotle University Thessaloniki | ||||||||||||||||||
Full Title: A randomised, double blind, placebo-controlled study of the effect of liraglutide on arterial blood pressure in hypertensive patients with type 2 diabetes mellitus | ||||||||||||||||||
Medical condition: Hypertention, Type 2 Diabetes | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: GR (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2009-012966-30 | Sponsor Protocol Number: DSE-SEV-02-09 | Start Date*: 2009-11-16 | |||||||||||
Sponsor Name:DAIICHI SANKYO EUROPE GmbH | |||||||||||||
Full Title: Eficacia de Sevikar® comparado con la combinación de Perindoprilo/Amlodipino sobre la Presión Arterial Central, en Pacientes con Hipertensión moderada a severa - SEVITENSION | |||||||||||||
Medical condition: Eficacia de Sevikar® comparado con la combinación de Perindoprilo/Amlodipino sobre la Presión Arterial Central, en Pacientes con Hipertensión moderada a severa - SEVITENSION | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-004300-35 | Sponsor Protocol Number: ikfe-Lina-003 | Start Date*: 2013-01-17 | ||||||||||||||||
Sponsor Name:Profil Mainz GmbH & Co KG | ||||||||||||||||||
Full Title: Effects of Linagliptin on Endothelial- , Renal-, and Retinal Function in Comparison to Placebo in Patients with Hypertension and Albuminuria | ||||||||||||||||||
Medical condition: Linagliptin in Patients with Hypertension and Albuminuria | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Completed) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2017-000137-31 | Sponsor Protocol Number: 2017-2019 | Start Date*: 2017-12-19 | ||||||||||||||||
Sponsor Name:VU University Medical Center | ||||||||||||||||||
Full Title: Pulmonary Hypertension REversal in Clusters of Patients With Identical Pathobiological Substrates. 6-Mercaptopurine Proof-of-Concept Trial | ||||||||||||||||||
Medical condition: Pulmonary arterial hypertension | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-003910-26 | Sponsor Protocol Number: 01/2015 | Start Date*: 2017-12-11 |
Sponsor Name:Núcleo de Estudos de Hipertensão da Beira Interior | ||
Full Title: Fase II, unicenter, open, randomized trial to evaluate the response of Th17 and T regulatory lymphocytes to 24 weeks supplementation with cholecalciferol in patients with arterial hypertension, obe... | ||
Medical condition: Obesity associated arterial hypertension Metabolic syndrome associated arterial hypertension | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: PT (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2005-004579-39 | Sponsor Protocol Number: CSPP100A2332 | Start Date*: 2006-09-08 |
Sponsor Name:Novartis Pharma Services AG | ||
Full Title: An eight-week, randomized, double-blind, parallel-group, multicenter study to evaluate the efficacy and safety of the combination of aliskiren / HCTZ (300/12.5 mg and 300/25 mg) in comparison with ... | ||
Medical condition: Hypertension | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) IT (Completed) | ||
Trial results: View results |
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 |
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