- Trials with a EudraCT protocol (442)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (9)
442 result(s) found for: Stenosis.
Displaying page 1 of 23.
EudraCT Number: 2007-003162-17 | Sponsor Protocol Number: 04062007 | Start Date*: 2007-10-11 | |||||||||||
Sponsor Name:Markku Kupari | |||||||||||||
Full Title: Lääkehoito aorttaläpän stenoosin ehkäisyssä Angiotensiinireseptorin salpaajan vaikutukset stenoottisen aorttaläpän tulehdukseen, fibroosiin ja kalkkiutumiseen | |||||||||||||
Medical condition: Aorttaläpän stenoosi | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2005-005962-36 | Sponsor Protocol Number: inv driven trial with RVG26872 | Start Date*: 2006-03-22 |
Sponsor Name: | ||
Full Title: Prospective randomized trial of effects of rosuvastatin on the progression of stenosis in adult patients with congenital aortic stenosis | ||
Medical condition: congenital aortic stenosis | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: BE (Completed) | ||
Trial results: View results |
EudraCT Number: 2009-013259-31 | Sponsor Protocol Number: 6232 | Start Date*: 2009-12-29 | ||||||||||||||||
Sponsor Name:UMC Utrecht | ||||||||||||||||||
Full Title: A multicenter double blind placebo-controlled randomised trial for benign esophageal anastomotic strictures: Savary dilation vs savary dilation with Triamcinolon | ||||||||||||||||||
Medical condition: Patients with first time dysphagia (grade 2-4) due to a benign anastomotic esophageal stricture | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: NL (Completed) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2011-000111-26 | Sponsor Protocol Number: MEIN/10/Ran-Did/002 | Start Date*: 2011-07-01 | |||||||||||
Sponsor Name:A. MENARINI PHARMA U.K., | |||||||||||||
Full Title: Effect of late sodium current inhibition on MRI measured diastolic dysfunction and myocardial perfusion reserve in aortic stenosis - a proof of concept study. | |||||||||||||
Medical condition: Aortic stenosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2012-003391-39 | Sponsor Protocol Number: 9026 | Start Date*: 2012-10-26 | |||||||||||
Sponsor Name:University Hospital of Montpellier | |||||||||||||
Full Title: Ballon aortic valvuloplasty performed without heparin to decrease vascular and bleeding complications of the procedure | |||||||||||||
Medical condition: Aortic stenosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-002291-27 | Sponsor Protocol Number: RIVAR-CTP-01 | Start Date*: 2016-11-07 | |||||||||||
Sponsor Name:Aalborg University Hospital | |||||||||||||
Full Title: Randomized trial of aspirin versus rivaroxaban after replacement of the aortic valve with a biological valve prosthesis | |||||||||||||
Medical condition: Aortic valve stenosis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2010-018490-38 | Sponsor Protocol Number: 1616 | Start Date*: 2010-06-14 | ||||||||||||||||
Sponsor Name:Anæstesiologisk Afd. I, Skejby Sygehus | ||||||||||||||||||
Full Title: Effekten af levosimendan på systolisk deformation og diastolisk funktion hos patienter med operationskrævende aortastenose og svær hypertrofi af venstre ventrikel | ||||||||||||||||||
Medical condition: Aortaklapsstenose Diastolisk dysfunktion | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DK (Prematurely Ended) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2021-003927-13 | Sponsor Protocol Number: REAC-TAVI2 | Start Date*: 2021-10-15 | |||||||||||||||||||||
Sponsor Name:Fundación Biomédica Galicia Sur | |||||||||||||||||||||||
Full Title: Single antiplatelet therapy with Ticagrelor vs Aspirin after Transcatheter Aortic Valve Implantation: multicenter randomized clinical trial. REAC TAVI 2 | |||||||||||||||||||||||
Medical condition: Symptomatic severe aortic stenosis | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-005856-33 | Sponsor Protocol Number: AT10008 | Start Date*: 2007-02-13 | |||||||||||
Sponsor Name:The Department of Molecular Medicin and Surgery, P9:03, Karolinska Institutet | |||||||||||||
Full Title: Local Glucocorticoid Injektion in the Treatment of Benign Oesophageal Strictures, a Randomized Clinical Study | |||||||||||||
Medical condition: Patients with benign oesophageal strictures and symptoms where dilatation of the stricture is planned. | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: SE (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-001853-41 | Sponsor Protocol Number: 57698 | Start Date*: 2018-09-19 | ||||||||||||||||||||||||||
Sponsor Name:Academic Medical Center | ||||||||||||||||||||||||||||
Full Title: Intensive endoscopic therapy versus conventional treatment for untreated benign anastomotic strictures after esophagectomy: a pilot and randomized controlled trial | ||||||||||||||||||||||||||||
Medical condition: Benign esophagogastric anastomotic strictures after esophagectomy | ||||||||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: NL (Prematurely Ended) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-002799-18 | Sponsor Protocol Number: ICICOR-2017-01 | Start Date*: 2017-12-27 | |||||||||||
Sponsor Name:José Alberto San Román Calvar | |||||||||||||
Full Title: Renin-angiotensin System Blockade Benefits in Clinical Evolution and Ventricular Remodeling After Transcatheter Aortic Valve Implantation (RASTAVI) | |||||||||||||
Medical condition: Severe aortic stenosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: ES (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2007-007085-38 | Sponsor Protocol Number: 1012007 | Start Date*: 2008-05-05 | |||||||||||
Sponsor Name:Kuopio University Hospital | |||||||||||||
Full Title: Estääkö postoperatiivisesti annettu kortikosteroidi hiippaläppäleikkauksen jälkeisen eteisvärinän ilmaantumista? | |||||||||||||
Medical condition: Tutkimukseen otetaan 220 peräkkäistä hiippaläppäleikkaukseen tulevaa potilasta, joilla ennen leikkausta on sinusrytmi. Tutkimukseen valittavilla potilailla on siis sydämen hiippaläpän leikkaushoito... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FI (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2016-002015-17 | Sponsor Protocol Number: 2016-002015-17 | Start Date*: 2017-03-10 | |||||||||||
Sponsor Name:Odense University Hospital | |||||||||||||
Full Title: Low-flow Low-gradient Aortic Stenosis – Diagnostic Usefullness of Ivabradine | |||||||||||||
Medical condition: Aortic valve stenosis with reduced ejection fraction | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-004653-24 | Sponsor Protocol Number: ARBAS041218 | Start Date*: 2020-06-15 | |||||||||||
Sponsor Name:Odense Universitets Hospital | |||||||||||||
Full Title: Impact of an Angiotensin Receptor Blocker in Aortic Stenosis – A Randomized Controlled Trial | |||||||||||||
Medical condition: Aortic valve stenosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-000608-40 | Sponsor Protocol Number: No-DAPT-TAVI | Start Date*: 2018-07-06 | |||||||||||
Sponsor Name:AOU DI BOLOGNA POLICLINICO S.ORSOLA-MALPIGHI | |||||||||||||
Full Title: Aspirin versus Aspirin plus Clopidogrel in Patients Undergoing Transcatheter Aortic Valve Replacement: a Randomized Multicenter Study | |||||||||||||
Medical condition: valvular aortic stenosis submitted to TAVI | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-005296-18 | Sponsor Protocol Number: BI8021_5101 | Start Date*: 2007-08-27 | ||||||||||||||||
Sponsor Name:Heinrich-Heine-Universität Duesseldorf | ||||||||||||||||||
Full Title: Einsatz von Haemateâ HS bei Patienten mit schweren Blutungskomplikationen bei Herzklappenersatz wegen Aortenstenose HAVAS-Studie (Haemate HS in patients with severe bleeding undergoing valve repl... | ||||||||||||||||||
Medical condition: Intraoperative Blutungsneigung während des Aortenklappenersatzes bei Patienten mit isolierter valvulärer Aortenstenose oder kombiniertem Aortenvitium mit führender Stenose Klassifikationscode ICD1... | ||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
Trial protocol: DE (Prematurely Ended) | ||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-005630-21 | Sponsor Protocol Number: D5130C00173 | Start Date*: 2016-06-30 | |||||||||||
Sponsor Name:National and Kapodistrian University of Athens | |||||||||||||
Full Title: A Prospective, Multicentre, Randomized, Open Label, Blinded Endpoint, Phase 3 Trial to Assess the Safety and Efficacy of Prophylactic TicagrelOr with Acetylsalicylic Acid versus CLopidogrel with Ac... | |||||||||||||
Medical condition: Preventing cerebrovascular embolic events during the TAVI procedure | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GR (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2008-002650-38 | Sponsor Protocol Number: Pre65 | Start Date*: 2008-07-01 | |||||||||||||||||||||
Sponsor Name:Organisation name was not entered | |||||||||||||||||||||||
Full Title: Vähentääkö pregabaliini opioidikipulääkityksen tarvetta ja kroonisen kivun esiintyvyyttä alle 65-vuotiailla potilailla sydänleikkauksen jälkeen? | |||||||||||||||||||||||
Medical condition: Tutkimukseen otetaan potilaan suostumuksella alle 65-vuotiaita avosydänleikkauk-seen joko koronaariohitus- tai sydämen läppärekonstruktioon tulevia potilaita, jotka leikatataan perfuusioleikkauksena. | |||||||||||||||||||||||
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Population Age: Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: FI (Completed) | |||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2006-000929-59 | Sponsor Protocol Number: MultiH/BRA/708 | Start Date*: Information not available in EudraCT | |||||||||||
Sponsor Name:Bracco ALTANA Pharma GmbH | |||||||||||||
Full Title: INTRAINDIVIDUAL CROSS-OVER STUDY TO COMPARE MULTIHANCE® AND MAGNEVIST® AT A DOSE OF 0.1 MMOL/KGBW IN CERVICO-CEREBRAL MR ANGIOGRAPHY AND CEREBRAL MR PERFUSION IMAGING AT 3 TESLA IN PATIENTS WITH CA... | |||||||||||||
Medical condition: Carotid artery stenosis and scheduled for MRA, for MR perfusion examination and for an elective stent treatment | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-007041-39 | Sponsor Protocol Number: IOP-108 | Start Date*: 2008-12-18 | |||||||||||
Sponsor Name:BRACCO IMAGING | |||||||||||||
Full Title: A Phase II Multicenter Randomized Double-Blind Dose-Finding Study of Iopamidol Injection 370 in Multidetector Computed Tomographic Angiography (MDCTA) in Patients with Suspected Coronary Artery Ste... | |||||||||||||
Medical condition: Patients who have known or suspected CAD and suspected significant (> 50%) coronary artery stenosis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
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