- Trials with a EudraCT protocol (21)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
21 result(s) found for: Radial artery.
Displaying page 1 of 2.
| EudraCT Number: 2017-000321-12 | Sponsor Protocol Number: 001/2016 | Start Date*: 2018-02-08 | |||||||||||
| Sponsor Name:ÁREA DE ATENCIÓN INTEGRADA DE ALBACETE | |||||||||||||
| Full Title: Effectiveness in preventing RAdial Spasm of different vasoDIlators and topic Local Anaesthesia during transradial cardiac catheterization: The E-RADIAL trial. | |||||||||||||
| Medical condition: Radial spasm during cardiac catheterization | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2007-000510-37 | Sponsor Protocol Number: GTN-1 290107 | Start Date*: 2008-04-25 |
| Sponsor Name:Nottingham Univeristy Hospitals NHS Trust | ||
| Full Title: The effect of transdermal GTN on arterial size and procedure outcomes in transradial coronary angiography - pilot study. | ||
| Medical condition: The trial is to investigate whether applying a transdermal GTN patch over the radial artery reduces spasm of the artery during coronary angiography. This is a pilot study | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: GB (Prematurely Ended) | ||
| Trial results: View results | ||
| EudraCT Number: 2012-005410-19 | Sponsor Protocol Number: HH-AT-001 | Start Date*: 2013-03-11 | |||||||||||
| Sponsor Name:Jessaziekenhuis Hasselt | |||||||||||||
| Full Title: Developing a Patient Model of Controlled, Radial Artery Access Site Bleeding for Deciding on Anticoagulation Reversal in Patients Treated by Systemic Anticoagulants. | |||||||||||||
| Medical condition: With the novel oral anticoagulants, including EDOXABAN-DABIGATRANRIVAROXABAN- APIXABAN, we are entering a new era of anticoagulation for atrial fibrillation (AF) (and deep vein thrombosis). Neve... | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Prematurely Ended) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2011-004779-35 | Sponsor Protocol Number: CL2-16257-096 | Start Date*: 2012-04-20 | |||||||||||
| Sponsor Name:Institut de Recherches Internationales Servier | |||||||||||||
| Full Title: Effects of oral chronic administration of ivabradine (7.5 mg bid) in comparison to placebo (bid) on top of beta-blockers, on central aortic blood pressure. Randomized, cross-over, double blind, mul... | |||||||||||||
| Medical condition: Coronary Artery Disease | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IE (Prematurely Ended) IT (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2014-002796-28 | Sponsor Protocol Number: CEASESTIFFNESS | Start Date*: 2016-04-12 |
| Sponsor Name:University Medical Center Groningen (UMCG) | ||
| Full Title: The Clinical Efficacy And Subclinical Effects on arterial STIFFNESS of bosentan therapy added to usual care in patients with systemic sclerosis with digital ulcers. | ||
| Medical condition: Systemic sclerosis (SSc) is characterized by skin fibrosis and visceral disease, mainly of the lungs, kidneys and the heart, accompanied by microvascular damage ultimately leading to digital ischem... | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: NL (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2015-002488-40 | Sponsor Protocol Number: LIPMAT | Start Date*: 2015-11-06 | |||||||||||
| Sponsor Name:Leiden University Medical Center | |||||||||||||
| Full Title: The LIPMAT study: Liposomal prednisolone to improve hemodialysis fistula maturation | |||||||||||||
| Medical condition: Nonmaturation of arteriovenous vascular accesses for hemodialysis. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: NL (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2020-000661-16 | Sponsor Protocol Number: CGRP2020 | Start Date*: 2020-06-18 | |||||||||||||||||||||
| Sponsor Name:Rigshospitalet Glostrup | |||||||||||||||||||||||
| Full Title: The effect of anti-calcitonin gene-related peptide (CGRP) receptor antibodies on the headache inducing properties of CGRP and cilostazol in migraine patients | |||||||||||||||||||||||
| Medical condition: Migraine | |||||||||||||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
| Trial protocol: DK (Completed) | |||||||||||||||||||||||
| Trial results: View results | |||||||||||||||||||||||
| EudraCT Number: 2011-000833-35 | Sponsor Protocol Number: CRLX030A2201 | Start Date*: 2011-10-24 | |||||||||||
| Sponsor Name:Novartis Pharma Services AG | |||||||||||||
| Full Title: A multicenter, phase II, double blind, randomized, parallel group, placebo-controlled study to evaluate the hemodynamic responses to intravenous RLX030 infusion in subjects with acute heart failure. | |||||||||||||
| Medical condition: Acute Heart Failure | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) PL (Completed) IT (Completed) NL (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2017-000934-77 | Sponsor Protocol Number: 4.0 | Start Date*: 2018-05-11 |
| Sponsor Name:Medical University of Vienna | ||
| Full Title: Target attainment of Cefazolin Continuous Infusion for Antibiotic Prophylaxis in patients undergoing CABG surgery | ||
| Medical condition: Patients referred for CABG to the Department of Cardiac Surgery with planned isolated left mammary artery and vein/radial artery grafts preparation will be asked to participate in this trial. | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: AT (Completed) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2008-008713-20 | Sponsor Protocol Number: BGC20-1531-04 | Start Date*: 2009-03-26 |
| Sponsor Name:Danish Headache Center | ||
| Full Title: EP4 receptor antagonism and PGE2 in a human headache model | ||
| Medical condition: PGE2 will induce headache in healthy subjects and BGC20-1531 or placebo will be used to block the developement of headache. In the future BGC20-1531 might be a possible anti-migraine drug. | ||
| Disease: | ||
| Population Age: Adults | Gender: Male, Female | |
| Trial protocol: DK (Prematurely Ended) | ||
| Trial results: View results | ||
| 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: 2006-000313-38 | Sponsor Protocol Number: EFC5965 | Start Date*: 2007-01-24 | |||||||||||
| Sponsor Name:Sanofi-aventis Recherche & Développement | |||||||||||||
| Full Title: Randomized, multinational, double-blind study, comparing a high loading dose regimen of clopidogrel versus standard dose in patients with unstable angina or myocardial infarction managed with an ea... | |||||||||||||
| Medical condition: Patients with non-ST segment elevation myocardial infarction managed with an early PCI. | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) CZ (Completed) FI (Completed) IE (Completed) SK (Completed) FR (Completed) SE (Completed) DE (Completed) AT (Completed) EE (Completed) BG (Completed) GR (Completed) IT (Completed) GB (Completed) LT (Completed) NL (Completed) LV (Completed) ES (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2013-000030-35 | Sponsor Protocol Number: RIMINI-Pilot | Start Date*: 2013-05-08 | |||||||||||
| Sponsor Name:University Medical Center Hamburg-Eppendorf | |||||||||||||
| Full Title: Reduction of Ischemic Myocardium with Ranolazine-Treatment in patients with acute myocardial Ischemia – RIMINI-Pilot-Trial | |||||||||||||
| Medical condition: CAD with acute ischemia and myocardial dysfunction | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2009-011662-28 | Sponsor Protocol Number: ABRACADABRA | Start Date*: 2009-11-26 | |||||||||||
| Sponsor Name:AZIENDA OSPEDALIERA SAN GERARDO DI MONZA | |||||||||||||
| Full Title: Exploratory study on inflammatory immune response related to endothelial dysfunction in HIV-infected na�ve patients treated with abacavir compared to tenofovir-based regimens. | |||||||||||||
| Medical condition: HIV INFECTION | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2021-002893-20 | Sponsor Protocol Number: 2021/0188/HP | Start Date*: 2021-12-03 | |||||||||||
| Sponsor Name:CHU de Rouen | |||||||||||||
| Full Title: Impact of dapagliflozin on vascular function in chronic kidney disease patients | |||||||||||||
| Medical condition: chronic kidney disease patients | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Trial now transitioned) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2010-018774-21 | Sponsor Protocol Number: MeIn/08/OLMAML-Hyp/001 | Start Date*: 2010-08-04 | |||||||||||
| Sponsor Name:MENARINI INTERNATIONAL OPERATIONS LUXEMBOURG SA | |||||||||||||
| Full Title: Tratamiento con Olmesartán + Amlodipino en pacientes diabéticos: evaluación del control de la presión sanguínea 48 horas después de la última administración (dosis omitida) | |||||||||||||
| Medical condition: Hipertensión | |||||||||||||
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| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) FR (Completed) DE (Completed) GR (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2007-005911-25 | Sponsor Protocol Number: 001 | Start Date*: 2008-10-10 | ||||||||||||||||||||||||||||||||||||
| Sponsor Name:Imperial College Healthcare NHS Trust | ||||||||||||||||||||||||||||||||||||||
| Full Title: A randomised, placebo controlled, double blind study to evaluate the effect of 300mcg testosterone patches in addition to HRT on arterial compliance, insulin resistance and sexual desire. | ||||||||||||||||||||||||||||||||||||||
| Medical condition: - arterial compliance - insulin resistance - decreased sexual desire after menopause | ||||||||||||||||||||||||||||||||||||||
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| Population Age: Adults, Elderly | Gender: Female | |||||||||||||||||||||||||||||||||||||
| Trial protocol: GB (GB - no longer in EU/EEA) | ||||||||||||||||||||||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||||||||||||||||||||||
| EudraCT Number: 2017-002268-42 | Sponsor Protocol Number: 205767 | Start Date*: 2018-03-29 | |||||||||||
| Sponsor Name:GlaxoSmithKline Research & Development Ltd | |||||||||||||
| Full Title: A randomized, repeat dose, open label, parallel group, multi-center study to evaluate the effect of daprodustat compared to darbepoetin alfa on forearm blood flow in participants with anemia of chr... | |||||||||||||
| Medical condition: anemia associated with chronic kidney disease | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: GB (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-006644-19 | Sponsor Protocol Number: CRISTAL | Start Date*: 2009-01-29 | |||||||||||
| Sponsor Name:AZIENDA OSPEDALIERA SAN GERARDO DI MONZA | |||||||||||||
| Full Title: Evaluation of inflammatory immune parameters predicting cardiovascular risk in HIV-1-infected antiretroviral therapy naive patients treated with atazanavir/ritonavir versus lopinavir/ritonavir base... | |||||||||||||
| Medical condition: HIV infection | |||||||||||||
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| Population Age: Adults | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2017-001547-12 | Sponsor Protocol Number: DC2017RACELINES01 | Start Date*: 2017-12-21 |
| Sponsor Name:VU University Medical Center | ||
| Full Title: A phase 4, monocenter, randomized, double-blind, comparator-controlled, 3-armed parallel mechanistic intervention trial to assess the effect of 8-week empagliflozin (SGLT-2 inhibitor) monotherapy, ... | ||
| Medical condition: Type 2 Diabetes Mellitus | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: NL (Completed) | ||
| Trial results: (No results available) | ||
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