- Trials with a EudraCT protocol (202)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
202 result(s) found for: Coronary Artery Disease (CAD).
Displaying page 5 of 11.
| EudraCT Number: 2006-000192-14 | Sponsor Protocol Number: TMC-CAN-05-02 | Start Date*: 2006-12-21 | |||||||||||
| Sponsor Name:The Medicines Company | |||||||||||||
| Full Title: A Clinical Trial Comparing Cangrelor To Clopidogrel In Subjects Who Require Percutaneous Coronary Intervention | |||||||||||||
| Medical condition: Subjects with coronary atherosclerosis who require PCI (with or without stent). | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: AT (Prematurely Ended) ES (Completed) DE (Completed) IT (Completed) GB (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2004-005002-68 | Sponsor Protocol Number: DXV405 | Start Date*: 2005-11-03 | |||||||||||
| Sponsor Name:Amersham Health SA (Parte de GE Healthcare Ltd. y sus filiales) | |||||||||||||
| Full Title: Estudio multicéntrico, aleatorizado, doble ciego, paralelo y de fase IV para comparar los efectos en la función renal del medio de contraste no iónico, isosmolar, iodixanol 320 mgI/ml (VisipaqueTM)... | |||||||||||||
| Medical condition: Subjects with impaired renal function and diabetes mellitus undergoing coronary angiography. | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2019-002226-79 | Sponsor Protocol Number: AUGEAS | Start Date*: Information not available in EudraCT | ||||||||||||||||||||||||||
| Sponsor Name:Region Skåne | ||||||||||||||||||||||||||||
| Full Title: A 30-day, randomized, evalUator-blind, controlled, multi-centre, parallel Group, phase III study to evaluate the Effect of a Low Maintenance Dose TicAgrelor Regimen versus Standard Dose Clopidogrel... | ||||||||||||||||||||||||||||
| Medical condition: Coronary Artery Disease (CAD) | ||||||||||||||||||||||||||||
|
||||||||||||||||||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||||||||||||
| Trial protocol: SE (Prematurely Ended) IT (Prematurely Ended) | ||||||||||||||||||||||||||||
| Trial results: View results | ||||||||||||||||||||||||||||
| EudraCT Number: 2021-002557-29 | Sponsor Protocol Number: SK_DMDPA-03 | Start Date*: 2021-10-25 | |||||||||||
| Sponsor Name:Synektik Spółka Akcyjna | |||||||||||||
| Full Title: A Phase III Study of [11C]-DMDPA Tracer for Positron Emission Tomography PET-CT Myocardial Perfusion Imaging (MPI). | |||||||||||||
| Medical condition: Known or suspected acute coronary syndrome | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: PL (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2011-000190-31 | Sponsor Protocol Number: MEDCOR2011 | Start Date*: 2011-05-27 | ||||||||||||||||
| Sponsor Name:Therabel Pharmaceuticals Ltd | ||||||||||||||||||
| Full Title: Double-blind parallel placebo-controlled study to evaluate the effect of Molsidomine on the Endothelial Dysfunction in patients with stable angina pectoris undergoing a percutaneous CORonary interv... | ||||||||||||||||||
| Medical condition: Patients with stable angina undergoing elective PCI, used an add-on treatment on standard care therapy, molsidomine or placebo to improve the endothelial function (12 months treatment) | ||||||||||||||||||
|
||||||||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: BE (Completed) | ||||||||||||||||||
| Trial results: Removed from public view | ||||||||||||||||||
| EudraCT Number: 2007-007723-40 | Sponsor Protocol Number: 0974-034 | Start Date*: 2008-04-25 | ||||||||||||||||
| Sponsor Name:Merck Sharp & Dohme (Europe) Inc. | ||||||||||||||||||
| Full Title: A Multicenter, Randomized, Double-Blind, Active- and Placebo-Controlled, Period Crossover Study to Evaluate the Safety and Efficacy of MK-0974 in the Treatment of Acute Migraine in Patients With St... | ||||||||||||||||||
| Medical condition: migraine, coronary artery disease | ||||||||||||||||||
|
||||||||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: BE (Completed) AT (Completed) IT (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2021-000823-11 | Sponsor Protocol Number: TIMO | Start Date*: 2023-03-09 | ||||||||||||||||
| Sponsor Name:Sahlgrenska University Hospital Gothenburg | ||||||||||||||||||
| Full Title: Ticagrelor monotherapy after coronary stenting in patients with acute myocardial infarction. A prospective single-centre, single-arm phase II study | ||||||||||||||||||
| Medical condition: Antiplatelet therapy in patients who undergo coronary artery stenting due to coronary artery disease (CAD) or acute coronary syndrome (ACS). The present study will examine whether ticagrelor, as mo... | ||||||||||||||||||
|
||||||||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: SE (Trial now transitioned) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2015-004825-14 | Sponsor Protocol Number: D1680C00016 | Start Date*: 2016-05-04 | |||||||||||
| Sponsor Name:AstraZeneca AB | |||||||||||||
| Full Title: A 24-Week, Multicenter, Randomized, Double-blind, Parallel Group, Placebo-controlled Study to Investigate the Effects of Saxagliptin, Saxagliptin Combined with Dapagliflozin, and Sitagliptin in Pat... | |||||||||||||
| Medical condition: Patients with type 2 diabetes mellitus and heart failure | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Prematurely Ended) HU (Completed) BG (Completed) RO (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2005-001890-83 | Sponsor Protocol Number: P03573 | Start Date*: 2006-03-09 |
| Sponsor Name:Schering-Plough Research Institute | ||
| Full Title: A Multicenter, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Safety of SCH 530348 in Subjects Undergoing Non-Emergent Percutaneous Coronary Intervention (Thrombin Receptor Anta... | ||
| Medical condition: Subjects with symptoms of Coronary Heart Disease | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: SE (Prematurely Ended) BE (Completed) IT (Completed) DE (Completed) | ||
| Trial results: View results | ||
| EudraCT Number: 2011-001245-32 | Sponsor Protocol Number: PGX-III-AP-002 | Start Date*: 2011-10-19 | |||||||||||
| Sponsor Name:Forest Laboratories, Inc. | |||||||||||||
| Full Title: A Phase 3, Randomized, Double-Blind Trial of Apadenoson for the Detection of Myocardial Perfusion Defects Using Single-Photon Emission Computed Tomography (SPECT) Myocardial Perfusion Imaging (MPI) | |||||||||||||
| Medical condition: Coronary Artery Disease | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: BE (Completed) NL (Prematurely Ended) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2006-001430-40 | Sponsor Protocol Number: 012-06 | Start Date*: 2007-05-04 |
| Sponsor Name:University Hospital Department of Cardiology | ||
| Full Title: Tiral of Invasive versus Medical therapy of Early coronary artery disease in Diabetes (TIME-DM) | ||
| Medical condition: The prevalence of type II diabetes is increasing rapidly, contributing importantly to a new "epidemic" of coronary artery disease (CAD). Atherosclerosis accounts for 65-80% of all death among diabe... | ||
| Disease: | ||
| Population Age: Adults, Elderly | Gender: Male, Female | |
| Trial protocol: DE (Ongoing) | ||
| Trial results: (No results available) | ||
| EudraCT Number: 2022-002589-34 | Sponsor Protocol Number: FLECA-ED | Start Date*: 2022-12-16 | ||||||||||||||||
| Sponsor Name:WinMedica S.A. | ||||||||||||||||||
| Full Title: Μία προοπτική, πολυκεντρική, τυχαιοποιημένη, κλινική δοκιμή για την ασφάλεια και την αποτελεσματικότητα της Φλεκαϊνίδης έναντι της Αμιωδαρόνης για την καρδιοανάταξη της παροξυσμικής Κολπικής Μαρμαρ... | ||||||||||||||||||
| Medical condition: Καρδιοανάταξη της παροξυσμικής κολπικής μαρμαρυγής στο Τμήμα Επειγόντων Περιστατικών σε ασθενείς με στεφανιαία νόσο χωρίς υπολειπόμενη ισχαιμία και κλάσμα εξώθησης > 35%. | ||||||||||||||||||
|
||||||||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: GR (Trial now transitioned) | ||||||||||||||||||
| Trial results: (No results available) | ||||||||||||||||||
| EudraCT Number: 2011-002507-15 | Sponsor Protocol Number: GS-US-259-0116 | Start Date*: 2012-06-22 | |||||||||||
| Sponsor Name:Gilead Sciences, Inc. | |||||||||||||
| Full Title: A Phase 3, Randomized, Double-Blind, Placebo-Controlled Study of the Effects of Ranolazine on Major Adverse Cardiovascular Events in Subjects with a History of Chronic Angina Who Undergo Percutaneo... | |||||||||||||
| Medical condition: Coronary artery disease | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) SE (Completed) CZ (Completed) AT (Completed) GB (Completed) BE (Completed) NL (Completed) ES (Completed) IT (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2011-001488-40 | Sponsor Protocol Number: CCFMS181/211 | Start Date*: 2011-09-01 | |||||||||||
| Sponsor Name:FONDAZIONE MONZINO CENTRO CARDIOLOGICO | |||||||||||||
| Full Title: Antiplatelet effect of low doses of aspirin taken every 12 hours in patients undergoing coronary artery bypass graft and / or aortic valve replacement surgery with bioprostheses | |||||||||||||
| Medical condition: Coronary Atheroclerosis | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: IT (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2005-003013-32 | Sponsor Protocol Number: GE IDE No. A01005 | Start Date*: 2005-11-08 | |||||||||||
| Sponsor Name:Deutsches Herzzentrum München | |||||||||||||
| Full Title: PROSPECTIVE, RANDOMIZED, DOUBLE-BLIND, ACTIVE-CONTROLLED; MULTICENTER TRIAL OF BIVALIRUDIN AND UN-FRACTIONATED HEPARIN IN PATIENTS UNDERGOING PERCUTANEOUS CORONARY INTERVENTIONS | |||||||||||||
| Medical condition: Coronary Artery Disease | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2012-001989-15 | Sponsor Protocol Number: HomRate04_2012 | Start Date*: 2012-09-17 | |||||||||||
| Sponsor Name:Universität des Saarlandes | |||||||||||||
| Full Title: A randomised, placebo controlled, double blind, cross-over, single center clinical Study to investigate the effect of heart rate reduction with ivabradine on endothelial function and vascular stiff... | |||||||||||||
| Medical condition: Stable coronary heart disease. | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: DE (Ongoing) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2008-006447-40 | Sponsor Protocol Number: CSPP100A2366 | Start Date*: 2009-02-23 | |||||||||||
| Sponsor Name:Novartis Farmacéutica | |||||||||||||
| Full Title: Estudio multicéntrico, aleatorizado, doble ciego, con grupos paralelos y de 104 semanas de duración, para evaluar la eficacia de aliskiren en la progresión de la aterosclerosis en pacientes con enf... | |||||||||||||
| Medical condition: Progresión de la aterosclerosis en pacientes con enfermedad arterial coronaria | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: ES (Completed) IT (Completed) FR (Completed) DE (Completed) BE (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
| EudraCT Number: 2008-001352-51 | Sponsor Protocol Number: 07-116 | Start Date*: 2009-01-23 | ||||||||||||||||
| Sponsor Name:Portola Pharmaceuticals Inc. | ||||||||||||||||||
| Full Title: A Randomized, Double-Blind, Active-Controlled Trial to Evaluate Intravenous and Oral PRT060128, a Selective and Reversible P2Y12-Receptor Inhibitor, vs. Clopidogrel, as a Novel Antiplatelet Therapy... | ||||||||||||||||||
| Medical condition: Adjunctive antiplatelet prior, during and after non-urgent percutaneous coronary intervention (PCI) in patients with coronary artery disease | ||||||||||||||||||
|
||||||||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | |||||||||||||||||
| Trial protocol: DE (Completed) AT (Completed) | ||||||||||||||||||
| Trial results: View results | ||||||||||||||||||
| EudraCT Number: 2017-002055-28 | Sponsor Protocol Number: SK-DMDPA-02 | Start Date*: 2017-10-13 | |||||||||||
| Sponsor Name:Synektik Spółka Akcyjna | |||||||||||||
| Full Title: Safety and dose optimization for [11C] DMDPA as a PET imaging agent for evaluation of myocardial perfusion in subjects with known or suspected coronary artery disease (CAD). | |||||||||||||
| Medical condition: known or suspected coronary artery disease | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: PL (Completed) | |||||||||||||
| Trial results: (No results available) | |||||||||||||
| EudraCT Number: 2014-000457-36 | Sponsor Protocol Number: 14-006 | Start Date*: 2015-03-10 | |||||||||||
| Sponsor Name:CHU CAEN | |||||||||||||
| Full Title: A comparative dynamic study of myocardial perfusion reserve explored by cardiac WATER labelled O-15 -PET vs Tc99mibi D-SPECT in coronAry arterY disease. Protocol WATER -DAY | |||||||||||||
| Medical condition: Patient suspect d’une maladie coronaire et/ou syndrome coronarien ST- | |||||||||||||
|
|||||||||||||
| Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
| Trial protocol: FR (Completed) | |||||||||||||
| Trial results: View results | |||||||||||||
Subscribe to this Search
To subscribe to the RSS feed for this search click here
.
This will provide an RSS feed for clinical trials matching your search that have been added or updated in the last 7 days.
To subscribe to the RSS feed for this search click here
.
This will provide an RSS feed for clinical trials matching your search that have been added or updated in the last 7 days.
| Download Options: | |
|---|---|
| Number of Trials to download: | |
| Download Content: | |
| Download Format: | |
| Note, where multi-state trials are shown in search results, selecting "Full Trial details" will download full information for each of the member states/countries involved in the trial. | |
Query did not match any studies.