- Trials with a EudraCT protocol (67)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (1)
67 result(s) found for: Intima-media thickness.
Displaying page 1 of 4.
EudraCT Number: 2004-004463-30 | Sponsor Protocol Number: ATS K015 | Start Date*: 2005-06-22 |
Sponsor Name:Takeda Pharma GmbH | ||
Full Title: Effects of Pioglitazone in Combination with Atorvastatin in Comparison to Atorvastatin treatment alone on Intima-Media Thickness in patients at Risk for Vascular Complications | ||
Medical condition: Patients at risk for vascular complications (cardiovascular anamnesis, hypertension, hypercholesterolemia) and a carotid intima media thickness >= 0.8 mm at least at one side will be eligible for t... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2006-004427-11 | Sponsor Protocol Number: 060317 | Start Date*: 2006-10-27 |
Sponsor Name:Univ of Lund, Dept of Pediatrics | ||
Full Title: Effects of Omega-3-Fatty Acids on Arterial Endothelial Function and Intima Media Thickness in Children with Insulin-Dependent Diabetes Mellitus | ||
Medical condition: Diabetes mellitus type 1 in children | ||
Disease: | ||
Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | |
Trial protocol: SE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2005-004421-26 | Sponsor Protocol Number: Leipzig-01 | Start Date*: 2006-07-18 |
Sponsor Name:Institut fuer Gesundheits- und Praxismanagement GmbH | ||
Full Title: Effect of Pioglitazone on Intima Media Thickness, Endothelial Function and Heart Rate Variability in Patients with Impaired Glucose Tolerance | ||
Medical condition: Impaired glucose tolerance | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Prematurely Ended) | ||
Trial results: (No results available) |
EudraCT Number: 2005-000129-47 | Sponsor Protocol Number: REUMAUMAS 2005-1 | Start Date*: 2005-03-21 |
Sponsor Name:Dept. of Rhematology UMAS | ||
Full Title: The effect of Adalimumab (Humira) on vascular abnormalities in rheumatoid arthritis. A pilot study. | ||
Medical condition: Rheumatoid Arthritis. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: SE (Completed) | ||
Trial results: (No results available) |
EudraCT Number: 2008-004224-23 | Sponsor Protocol Number: TSAIMT01 | Start Date*: 2009-03-13 | |||||||||||
Sponsor Name:University of Glasgow / NHS Greater Glasgow and Clyde | |||||||||||||
Full Title: The effect of allopurinol on carotid ultrasound intima-media thickness and markers of endothelial function in patients with recent stroke - a pilot study. | |||||||||||||
Medical condition: Ischaemic stroke or transient ischaemic attack (TIA) (ICD Classification Code I63.0-9 and G45.0-1). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2006-003001-49 | Sponsor Protocol Number: P05.020 | Start Date*: 2006-08-07 |
Sponsor Name:Leiden University Medical Center | ||
Full Title: Anti-inflammatory effects of rosiglitazone in patients with stage 4 and 5 chronic kidney disease | ||
Medical condition: Chronic kidney disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2010-023325-37 | Sponsor Protocol Number: CRO1656 | Start Date*: 2011-01-25 |
Sponsor Name:Imperial College | ||
Full Title: UMPIRE Trial sub-study - Polypill Effects on Sub Clinical Atherosclerosis (PESCA): A randomised controlled trial of a cardiovascular polypill treatment strategy compared with usual care on carotid ... | ||
Medical condition: Cardiovascular disease subjects either with established disease or at high risk | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2020-004391-18 | Sponsor Protocol Number: PI2020_843_0114 | Start Date*: 2020-10-28 |
Sponsor Name:CHU Amiens-Picardie | ||
Full Title: IMPACT OF ANTI-TNF, VEDOLIZUMAB AND TOFACITINIB ON AORTIC STIFFNESS, CAROTID INTIMA-MEDIA THICKNESS AND CARDIOVASCULAR RISK OF PATIENTS WITH ULCERATIVE COLITIS | ||
Medical condition: ulcerative colitis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: FR (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2011-003179-12 | Sponsor Protocol Number: MN0511_1 | Start Date*: 2012-01-09 |
Sponsor Name:University Hospital of Wuerzburg, Medical Director | ||
Full Title: Mineralocorticoid Receptor antagonists in End stage reNal DiseAse | ||
Medical condition: Hemodialysis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Completed) | ||
Trial results: View results |
EudraCT Number: 2012-004992-37 | Sponsor Protocol Number: 2012/1419 | Start Date*: 2013-02-25 |
Sponsor Name:South-Eastern Norway Regional Health Authority [...] | ||
Full Title: The effects of n-3 polyunsaturated fatty acids on glomerular filtration rate, proteinuria, fibrosis and inflammation in the kidney transplant and cardiovascular risk markers in kidney transplant re... | ||
Medical condition: Renal transplantation | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NO (Completed) | ||
Trial results: (No results available) |
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: 2012-001066-14 | Sponsor Protocol Number: DENERVHTA | Start Date*: 2012-07-17 |
Sponsor Name:Consorci Mar Parc de salut de Barcelona ( Parc de Salut Mar) | ||
Full Title: Sympathetic renal denervation versus increment of pharmacological treatment in resistant arterial hypertension | ||
Medical condition: subjects with resistant hypertension | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2005-005206-23 | Sponsor Protocol Number: 105 | Start Date*: 2006-11-03 |
Sponsor Name:3.Med. Department, Academic Hospital Bogenhausen | ||
Full Title: A randomized, therapy controlled, double blind, single center cross-over pilot study to evaluate the antihypertensive and pleiotropic effects of telmisartan in comparison to amlodipin on myocardial... | ||
Medical condition: patients with metabolic syndrome, mild to moderate hypertension and without overt coronary artery disease | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: DE (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2010-019656-41 | Sponsor Protocol Number: ZA/CP/0210 | Start Date*: 2011-08-24 | |||||||||||
Sponsor Name:King’s College London [...] | |||||||||||||
Full Title: Effects of Zoledronic Acid on arterial calcification and arterial stiffness in women – a co-twin randomised double blind, placebo-controlled parallel group, clinical trial | |||||||||||||
Medical condition: Arterial stiffness and arterial calcification | |||||||||||||
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Population Age: Adults, Elderly | Gender: Female | ||||||||||||
Trial protocol: GB (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-000981-12 | Sponsor Protocol Number: ALIROCKS_05MAR2018_V3 | Start Date*: 2018-05-11 |
Sponsor Name:Medical University of Graz | ||
Full Title: A PILOT STUDY INVESTIGATING THE EFFECTS OF LIPID-THERAPY INTENSIFICATION WITH ALIROCUMAB ON ENDOTHELIAL FUNCTION, CAROTID ARTERIES, LIPOPROTEIN PARTICLE SUBFRACTIONS, INFLAMMATION AND POST-PRANDIAL... | ||
Medical condition: Primary Hypercholesterolemia in secondary prevention after an acute atherosclerotic, ischaemic cardiovascular event for patients with diagnostically confirmed coronary heart disease and / or periph... | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: AT (Prematurely Ended) | ||
Trial results: View results |
EudraCT Number: 2021-000434-34 | Sponsor Protocol Number: UMCU-VASC-CO-003 | Start Date*: 2023-04-12 |
Sponsor Name:University Medical Centre Utrecht | ||
Full Title: A placebo-controlled, double-blind randomized trial evaluating the effect of etidronate in young patients with pseudoxanthoma elasticum on ectopic mineralization. | ||
Medical condition: Pseudoxanthoma elasticum | ||
Disease: | ||
Population Age: Adults | Gender: Male, Female | |
Trial protocol: NL (Trial now transitioned) | ||
Trial results: (No results available) |
EudraCT Number: 2004-005184-15 | Sponsor Protocol Number: 05_ENDO_46 | Start Date*: 2005-05-24 |
Sponsor Name:Christie Hospital NHS Trust | ||
Full Title: Central Hypothyroidism and Adjusted Thyroxine dose Study (CHATS): impact of increasing free thyroxine levels in patients with hypopituitarism | ||
Medical condition: Central (secondary/tertiary) hypothyroidism (subclinical) | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: GB (Completed) | ||
Trial results: View results |
EudraCT Number: 2008-002169-30 | Sponsor Protocol Number: GlaMet1 | Start Date*: 2008-09-19 | |||||||||||
Sponsor Name:Greater Glasgow Health Board, Research and Development Department [...] | |||||||||||||
Full Title: A randomised placebo-controlled trial of metformin on progression of carotid atherosclerosis in non-diabetic patients with cardiovascular disease treated with conventional risk reducing agents | |||||||||||||
Medical condition: Participants must have definite coronary heart disease: either a previous myocardial infarction or positive findings on coronary angiogram. They can have normal glucose tolerance, impaired fasting ... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2012-002583-27 | Sponsor Protocol Number: MCI-196-E15 | Start Date*: 2013-07-11 | |||||||||||
Sponsor Name:Mitsubishi Tanabe Pharma Corporation (MTPC) | |||||||||||||
Full Title: A Multi-centre, Flexible Dose, Parallel Group, Open-label, Active Control (Calcium-based Phosphate Binder), Long-term Extension Study Evaluating the Efficacy, Safety and Tolerability of Colestilan ... | |||||||||||||
Medical condition: Hyperphosphataemia | |||||||||||||
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Population Age: Children, Adolescents, Under 18 | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Prematurely Ended) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-002134-31 | Sponsor Protocol Number: HLS14/01 | Start Date*: 2015-07-22 |
Sponsor Name:Ospedale L. Sacco - Azienda Ospedaliera-Polo Universitario | ||
Full Title: Evalutation of maraviroc therapy in PI-treated HIV+ patients at intermediate-low risk for cardiovascular diseases: a phase IV, randomized, open study | ||
Medical condition: HIV-1 infection. | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: IT (Ongoing) | ||
Trial results: (No results available) |
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