- Trials with a EudraCT protocol (69)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
69 result(s) found for: Arterial insufficiency.
Displaying page 1 of 4.
| EudraCT Number: 2020-006121-65 | Sponsor Protocol Number: 65411807 | Start Date*: 2021-08-31 | |||||||||||
| Sponsor Name:Odense University Hospital | |||||||||||||
| Full Title: STUDY PROTOCOL: A multi-centre, randomized, double-blinded, placebo controlled 1-year study to compare the effect of hydrocortisone and palcebo in patients with partial adrenal insufficiency after ... | |||||||||||||
| Medical condition: To investigate the effects of hydrocortisone replacement in participants with previous PMR and GCA, who are in GC-free remission and exhibit biochemical evidence of mild to moderate adrenal insuffi... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DK (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2009-017625-20 | Sponsor Protocol Number: NAROSYD | Start Date*: 2010-06-22 | ||||||||||||||||
| Sponsor Name:Pawel Florkiewicz | ||||||||||||||||||
| Full Title: Continuous ropivacaine infusion in treatment of postoperative pain in cardiac surgery. | ||||||||||||||||||
| Medical condition: Research is to verify whether continuous infusion of ropivacaine reduces post-operative analgesic requirement after cardiac surgery. | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: FI (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2010-024417-31 | Sponsor Protocol Number: 2352 | Start Date*: 2011-03-11 |
| Sponsor Name:Beaumont Hospital/RCSI | ||
| Full Title: The effect of vitamin D replacement on arterial stiffness in an elderly community based population. | ||
| Medical condition: Vitamin D deficiency/insufficiency Arterial stiffness | ||
| Disease: | ||
| Population Age: Elderly | Gender: Male, Female | |
| Trial protocol: IE (Prematurely Ended) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2009-015005-39 | Sponsor Protocol Number: MW005 | Start Date*: 2009-11-03 | |||||||||||
| Sponsor Name:Dr. Willmar Schwabe GmbH & Co. KG | |||||||||||||
| Full Title: Monocentric prospective randomized controlled open phase IV study to explorate the mechanismen of the synergetic effect of the Crateagus -Extract WS® 1442 in addition to endurance training related ... | |||||||||||||
| Medical condition: heart failure, stage NYHA II | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2005-000115-10 | Sponsor Protocol Number: SPON CU 086 | Start Date*: 2005-10-14 |
| Sponsor Name:Cardiff University | ||
| Full Title: A randomised, double blind, placebo-controlled, cross-over study of the effects of dehydroepiandrosterone replacement on vascular function in patients with primary and secondary adrenal insufficiency. | ||
| Medical condition: Primary and secondary adrenal failure | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2012-000622-22 | Sponsor Protocol Number: ASAP | Start Date*: 2012-07-20 | |||||||||||
| Sponsor Name:Fundació Clínic per a la Recerca Biomèdica | |||||||||||||
| Full Title: Aspirin for the enhancement of trophoblastic invasion in women with abnormal uterine artery Doppler at 11-14 weeks of gestation | |||||||||||||
| Medical condition: Placental insufficiency | |||||||||||||
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| Population Age: Adults | Gender: Female | ||||||||||||
| Trial protocol: ES (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2022-003573-32 | Sponsor Protocol Number: 2022/ABM/01/00027 | Start Date*: 2023-12-28 | |||||||||||||||||||||||||||||||||||||||||
| Sponsor Name:Uniwersytet Medyczny im. Karola Marcinkowskiego w Poznaniu | |||||||||||||||||||||||||||||||||||||||||||
| Full Title: A randomized, double-blind, placebo-controlled study to evaluate the effect of allopurinol on the risk of cardiovascular events in patients at high and very high cardiovascular risk, including the ... | |||||||||||||||||||||||||||||||||||||||||||
| Medical condition: hyperuricemia, hypertension, ischemic stroke, intracerebral haemorrhage, TIA, heart failure, peripheral arterial disease, atrial fibrillation, diabetes mellitus | |||||||||||||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||||||||||||
| Trial protocol: PL (Trial now transitioned) | |||||||||||||||||||||||||||||||||||||||||||
| Trial results: (No results available) | |||||||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2017-005077-39 | Sponsor Protocol Number: BBLOQ-2017 | Start Date*: 2018-06-12 | |||||||||||
| Sponsor Name:Instituto de Investigación Sanitaria INCLIVA | |||||||||||||
| Full Title: Betablockers Withdrawal in Patients with Heart Failure with Preserved Ejection Fraction and Chronotropic Incompetence: Effect on Functional Capacity and life quality | |||||||||||||
| Medical condition: Heart Failure | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2006-001446-14 | Sponsor Protocol Number: N/GF-TORAFIC-06 | Start Date*: 2006-10-11 | |||||||||||
| Sponsor Name:NOVAG S.A., FERRER GRUPO | |||||||||||||
| Full Title: Multicenter parallel-group, concealed and randomized allocation and blinded-endpoint study, to evaluate the effects of Torasemide PR versus furosemide on a biochemical marker of collagen synthesis ... | |||||||||||||
| Medical condition: Heart failure | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2004-002122-22 | Sponsor Protocol Number: 02-VLU-003 | Start Date*: 2005-06-24 |
| Sponsor Name:Intercytex Limited | ||
| Full Title: A prospective, multi-centre, double blind, randomized, placebo controlled trial to evaluate the safety and efficacy of ICXP007 in a phase III trial with four-layer therapeutic compression, for trea... | ||
| Medical condition: Venous Insufficiency Leg Ulcers | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2012-002856-18 | Sponsor Protocol Number: RB12.079 | Start Date*: 2013-03-22 | ||||||||||||||||
| Sponsor Name:CHRU de Brest | ||||||||||||||||||
| Full Title: ALdosterone antagonist Chronic HEModialysis Interventional Survival Trial | ||||||||||||||||||
| Medical condition: | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: FR (Ongoing) BE (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2022-002688-31 | Sponsor Protocol Number: ICOR-2022-04-LEVOMEMS | Start Date*: 2023-01-25 | ||||||||||||||||||||||||||
| Sponsor Name:Germans Trias i Pujol Health Research Institute | ||||||||||||||||||||||||||||
| Full Title: LEVO-MEMS: COMPARISION OF THE HAEMODINAMIC PROFILE OF DOBUTAMIN AND LEVOSIMENDAN IN THE CURRENT THERAPEUTICAL CONTEXT | ||||||||||||||||||||||||||||
| Medical condition: Heart failure patients with depressed left ventricular ejection fraction | ||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: ES (Ongoing) | ||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||
| EudraCT Number: 2008-003676-22 | Sponsor Protocol Number: TMC-CLV-08-01 | Start Date*: 2009-04-01 | ||||||||||||||||
| Sponsor Name:The Medicines Company | ||||||||||||||||||
| Full Title: A Safety and Efficacy Study of Blood Pressure Control in Acute Heart Failure – A Pilot Study (PRONTO) | ||||||||||||||||||
| Medical condition: acute heart failure and elevated BP (systolic blood pressure [SBP] ≥160 mm Hg) requiring parenteral IV antihypertensive therapy | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DE (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2009-010280-17 | Sponsor Protocol Number: TSHYPE-2601-2009 | Start Date*: 2009-04-17 | ||||||||||||||||
| Sponsor Name:Organisation name was not entered | ||||||||||||||||||
| Full Title: TS HYPE - Turner syndrome and Hypertension; a double-blinded randomised interventional trial. | ||||||||||||||||||
| Medical condition: Turner syndrome, hypertension and aortopathy | ||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||
| Trial protocol: DK (Completed) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2014-001319-38 | Sponsor Protocol Number: MW051 | Start Date*: 2015-09-24 |
| Sponsor Name:Dr. Willmar Schwabe GmbH & Co. KG | ||
| Full Title: Monocenter prospective open single-arm phase IV study of the effects of hawthorn extract WS® 1442 on arterial micro-vascular structure and macro-vascular function, persistance and erectile functio... | ||
| Medical condition: Underlying cardiovascular disease | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male | |
| Trial protocol: DE (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2010-021258-20 | Sponsor Protocol Number: EAST | Start Date*: 2011-06-15 | ||||||||||||||||||||||||||||||||||||
| Sponsor Name:Kompetenznetz Vorhofflimmern e.V. (AFNET) | ||||||||||||||||||||||||||||||||||||||
| Full Title: Early treatment of Atrial fibrillation for Stroke prevention Trial (EAST) | ||||||||||||||||||||||||||||||||||||||
| Medical condition: Atrial fibrillation, stroke, heart failure, myocardial infarction, cognitive dysfunction | ||||||||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||||||||||||
| Trial protocol: DE (Completed) DK (Completed) NL (Completed) CZ (Completed) BE (Completed) ES (Completed) PL (Completed) IT (Ongoing) | ||||||||||||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2011-000805-27 | Sponsor Protocol Number: MEIN/10/Ran-Did/001 | Start Date*: 2012-10-23 | |||||||||||
| Sponsor Name:Menarini International Operations Luxembourg S.A., Avenue de la Gare, 1611 Luxembourg, Luxembourg | |||||||||||||
| Full Title: Effect of Ranolazine in Heart Failure Patients with Preserved Ejection Fraction | |||||||||||||
| Medical condition: Heart failure patients with preserved ejection fraction (HFpEF) | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Completed) ES (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-003104-39 | Sponsor Protocol Number: SIS-05-2013 | Start Date*: 2013-12-18 |
| Sponsor Name:Fakultní nemocnice Ostrava,Czech republic | ||
| Full Title: Randomised Clinical Study of Safety of Efficacy of Extracelular Matrix and Autologous Platelet Rich Plasma Concentrate for Wound Healing (Leg Ulcers Biodesign Wound Healing – LEGEND(A) Study) In... | ||
| Medical condition: Chronical ischemic and venous ulcers | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: CZ (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2018-004146-41 | Sponsor Protocol Number: 49RC18_0197 | Start Date*: 2019-01-30 | |||||||||||||||||||||||||||||||
| Sponsor Name:CHU Angers | |||||||||||||||||||||||||||||||||
| Full Title: First-BLINDOS - Evaluation d’une stratégie de dépistage systématique de la carence en vitamine D et du traitement en cas de déficit, sur l’amélioration de la distance maximale de marche chez les pa... | |||||||||||||||||||||||||||||||||
| Medical condition: Artériopathie oblitérante des membres inférieurs de stade 2 | |||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||||||||||||
| Trial protocol: FR (Completed) | |||||||||||||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||||||||||||
| EudraCT Number: 2013-004575-13 | Sponsor Protocol Number: TRAPS-1.5 | Start Date*: 2014-10-29 |
| Sponsor Name:Dipartimento di Scienze Cardiologiche, Toraciche e Vascolari-Università di Padova | ||
| Full Title: A prospective, randomized clinical trial comparing Rivaroxaban vs warfarin in high risk patients with antiphospholipid syndrome (TRAPS). | ||
| Medical condition: THROMBOEMBOLISM PREVENTION | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: IT (Prematurely Ended) | ||
| Trial results: (No results available) | ||
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