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Atherosclerosis clinical trials

View clinical trials related to Atherosclerosis.

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NCT ID: NCT03068078 Completed - Atherosclerosis Clinical Trials

A Reduced-carbohydrate Diet High in Monounsaturated Fats in Type 2 Diabetes

ReDuCtion
Start date: November 2016
Phase: N/A
Study type: Interventional

Further studies are needed to establish the optimal diet for treating T2D. The investigators wishes to investigate whether a low carbohydrate diet, high in monounsaturated fats (LCD) will affect cardiovascular function, metabolism and the liver. 135 participants with T2D, will be following either a LCD, or a regular diabetes diet (RDD) for 6 months. Measurements and investigations will be performed at baseline and after 6 months.

NCT ID: NCT03067441 Completed - Clinical trials for Hypercholesterolemia

Assessment of the Long-Term Safety and Efficacy of Bempedoic Acid (CLEAR Harmony OLE)

Start date: February 3, 2017
Phase: Phase 3
Study type: Interventional

The purpose of this study is to see if bempedoic acid (ETC-1002) is safe and well-tolerated in patients with high cardiovascular risk and elevated LDL cholesterol that is not adequately controlled by their current therapy.

NCT ID: NCT03064126 Completed - Atherosclerosis Clinical Trials

RANGER™ Paclitaxel Coated Balloon vs Standard Balloon Angioplasty

RANGER II SFA
Start date: March 2, 2017
Phase: Phase 3
Study type: Interventional

To evaluate the safety and effectiveness of the Ranger™ Paclitaxel Coated Balloon for treating lesions located in the superficial femoral and proximal popliteal arteries (SFA/PPA). Long Balloon substudy: To evaluate the safety and effectiveness of the Boston Scientific Corporation (BSC) Ranger™ Paclitaxel Coated Balloon in the 120, 150 and 200 mm lengths for treating Superficial Femoral Artery (SFA) and/or Proximal Popliteal Artery (PPA) lesions.

NCT ID: NCT03060577 Completed - Type2 Diabetes Clinical Trials

An Extension Trial of Inclisiran in Participants With Cardiovascular Disease and High Cholesterol

ORION-3
Start date: April 27, 2017
Phase: Phase 2
Study type: Interventional

This clinical study was designed to assess the efficacy, safety, and tolerability of long-term dosing of inclisiran and evolocumab given as subcutaneous injections in participants with high cardiovascular risk and elevated low-density lipoprotein cholesterol (LDL-C).

NCT ID: NCT03052582 Completed - Atherosclerosis Clinical Trials

Whole Milk Compared With Skimmed Milk and Effect on Lipids

Start date: October 2015
Phase: N/A
Study type: Interventional

The aim of the project is to investigate the effects in humans of a daily intake of whole milk compared to skimmed milk primarily and secondarily respectively on: - Blood lipids: total-, LDL-, and HDL-cholesterol and triglycerides - Risk markers of diabetes type 2: plasma glucose and insulin

NCT ID: NCT03048981 Completed - Surgery Clinical Trials

Effects of Fish Oil on Platelet Function and Coagulation

FOILP
Start date: March 1, 2017
Phase: N/A
Study type: Interventional

Many patients undergoing surgery use naturopathic drugs, including fish oil. Fish oil has been reported to increase bleeding in patients through inhibiting platelet aggregation and prolonging of clot formation time. The Swedish Medical Products Agency recommends that patients stop taking the naturopathic medicines including fish oil two weeks prior planed surgery. The aim of this study is to examine the effects of fish oil given to healthy volunteers using point of care coagulation assessment and flow dependent Cellix instrument before and after intake of fish oil.

NCT ID: NCT03044704 Active, not recruiting - Atherosclerosis Clinical Trials

Haemodynamic and Geometric Factors in Atherosclerosis

ANGLE
Start date: February 6, 2017
Phase:
Study type: Observational

The study is a prospective-observational, explorative single-centre cohort study aimed to examine the influence of hemodynamic and geometric parameters on the progression of atherosclerotic alterations in peripheral vessels (carotids, femoral artery). Atherosclerotic alterations (IMT, plaque volume) will be measured with a ultrasound (IMT measurements and 3D quantitative plaque volumetry) and magnetic resonance imaging (MRI). Geometric parameters (e.g. carotid/femoral bifurcation angle, carotid/femoral bifurcation area) are assessed with magnetic resonance imaging (MRI) and also 3D ultrasonography. A total of 100 patients with an asymmetrical plaque distribution in carotid and femoral arteries will be tested. Only patients who are already enrolled in the "Correlation of Artherosclerotic Plaque Volume and Intima Media Thickness With Soluble P-selectin" (NCT01895725) and who are tested prior for an asymmetrical plaque distribution will be included in this study. MRI will be performed once whereas ultrasound imaging will be be repeated once per year (up to five times) to assess changes in these parameters over time. Also plasma samples will be collected once yearly and tested for traditional and novel cardiovascular risk factors. The primary endpoint of the planned study will be the correlation between geometrical and hemodynamic parameters as stated above and the progression of atherosclerosis as measured by plaque volume and IMT in the carotid and femoral arteries, respectively. Secondary endpoints will include the correlation of geometrical and hemodynamic parameters with established (hypertension, smoking, diabetes, dyslipidemia) and novel risk factors (hsCRP, P-selectin, cholesteryl ester transfer protein (CETP), intercellular adhesion molecule-1 (ICAM-1), CETP TaqIb polymorphism), with cardiovascular event rate, plaque localization, plaque morphology and the additional predictive value of geometrical parameters compared to an established risk score (SCORE card).

NCT ID: NCT03042741 Recruiting - Atherosclerosis Clinical Trials

Vaccine Against Atherosclerosis in Patients With Overweight Problems or Obesity

V6
Start date: February 1, 2017
Phase: Phase 3
Study type: Interventional

Atherosclerosis vaccine, V6, has been through two small-scale Phase II open label clinical trials. It has shown significant improvement in lipid profile in patients with overweight or obesity

NCT ID: NCT03037411 Completed - Atherosclerosis Clinical Trials

A Real World Evaluation of the ELUVIA Stent in Subjects With Lesions Located in the Femoropopliteal Arteries

REGAL
Start date: December 13, 2016
Phase:
Study type: Observational

The REGAL study is a European, prospective, multi-center Post-Market Clinical Follow-up (PMCF) trial providing additional data including health economics data to support the use of the ELUVIA stent in the treatment of lesions located in the femoropopliteal arteries.

NCT ID: NCT03028025 Completed - Clinical trials for Coronary Artery Disease

Comparing TR Band to Statseal in Conjunction With TR Band

Start date: January 1, 2017
Phase: N/A
Study type: Interventional

The primary objectives of this study are to evaluate the performance of StatSeal Advanced used in conjunction with the TR Band (SSA) as compared to the TR Band without SSA (TRB) relative to: the incidence of peri-procedural radial artery occlusion (RAO) at discharge or 24 hours, whichever occurs first, and the Time to Hemostasis (TTH).