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Hypercholesterolemia clinical trials

View clinical trials related to Hypercholesterolemia.

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NCT ID: NCT04536870 Active, not recruiting - Heart Failure Clinical Trials

Statins in Reducing Events in the Elderly (STAREE) Heart Sub-study

STAREE-HEART
Start date: December 12, 2019
Phase: N/A
Study type: Interventional

The STAREE-HEART sub-study will examine the effect of statin treatment over a 3-year period compared with placebo on markers of cardiac ageing. This will include determining global longitudinal strain with transthoracic echocardiography, atrial fibrillation with home measures twice daily for two weeks and changes in biomarkers.

NCT ID: NCT04133805 Active, not recruiting - Clinical trials for Hypercholesterolemia

The Effect of Viscous Dietary Fibers on LDL-cholesterol

Start date: September 17, 2018
Phase:
Study type: Observational

This systematic review and meta-analysis is aimed to assess the effect of commonly consumed viscous fibers on blood lipids including LDL-C, non-HDL-C, and ApoB.

NCT ID: NCT04080050 Active, not recruiting - Clinical trials for Homozygous Familial Hypercholesterolemia (HoFH)

A Long-term Follow-up Study to Evaluate the Safety and Efficacy of RGX-501

Start date: September 30, 2019
Phase:
Study type: Observational

This long-term observational study is designed to follow subjects who, during another Clinical Study, received gene therapy treatment used to treat their Homozygous Familial Hypercholesterolemia (HoFH) disease. This study is intended to follow those subjects for up to 5 years since they received treatment to look for any long-term safety concerns. There is no investigational drug or therapy provided as part of this study.

NCT ID: NCT03952169 Active, not recruiting - Clinical trials for Primary Hypercholesterolemia

Effect of Probiotics on Lipid Management

Start date: May 12, 2019
Phase: N/A
Study type: Interventional

Dysbiosis of gut microbiota has been reported to be involved in the development of hypercholesterolemia in both humans and animal models. Probiotics have been reported to have ameliorative effects in murine models. However, whether probiotics could help alleviate dyslipidemia in adults remain obscure.

NCT ID: NCT03900169 Active, not recruiting - Clinical trials for Familial Hypercholesterolemia

Familial Hypercolerstremia as Risk Factor in Stemi Patient Who Underwent Ppci

Start date: November 1, 2020
Phase:
Study type: Observational

Famulial hypercolerstremia as risk factor

NCT ID: NCT03832985 Active, not recruiting - Clinical trials for Familial Hypercholesterolemia

Pediatric Reporting of Adult-Onset Genomic Results

Start date: November 25, 2020
Phase: Early Phase 1
Study type: Interventional

The Investigators will conduct a longitudinal, mixed-methods cohort study to assess primary and secondary psychosocial outcomes among 705 MyCode pediatric participants and their parents, and health behaviors of parents whose children receive an adult- or pediatric-onset genomic result. Data will be gathered via quantitative surveys using validated measures of distress, family functioning, quality of life, body image, perceived cancer/heart disease risk, genetic counseling satisfaction, genomics knowledge, and adjustment to genetic information; qualitative interviews with adolescents and parents; and electronic health records review of parents' cascade testing uptake and initiation of risk reduction behaviors. The investigators will also conduct empirical and theoretical legal research to examine the loss of chance doctrine and its applicability to genomic research.

NCT ID: NCT03469518 Active, not recruiting - Osteoporosis Clinical Trials

Effect of β-cryptoxanthin (β-Cx), Plant Sterols and Galactooligosaccharides on Systemic and Gastrointestinal Markers

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

Regular consumption of a beverage containing β-cryptoxanthin (β-Cx) and plant sterols (PS) has been shown to exert a synergic effect in reducing some markers of cardiovascular risk and bone-remodeling (formation and resorption). The present project aims to: - Evaluate (by in vivo and in vitro studies) the bioavailability of added β-Cx, PS and galactooligosaccharides (GOS) and its stability in the beverage employed in the proposed study. - Study the biological effect (bioefficacy) associated with the regular consumption of modified milk-based fruit beverages containing β-Cx, PS and GOS in post-menopausal women (target group) by assessing changes in inflammation, cardiovascular and bone turnover biochemical markers. - Characterize genetic variability (polymorphisms), genetic expression and DNA oxidative damage in the target group as determinants of bioavailability and biological effects of β-Cx, PS and GOS. - Evaluate the potential prebiotic effect associated to regular consumption of a beverage supplemented with β-Cx, PS and GOS: including "in vitro" studies and characterization of subjects' microbiota and possible microbiota changes associated to the beverage consumption.

NCT ID: NCT03464682 Active, not recruiting - Clinical trials for Primary Hypercholesterolemia

Efficacy and Safety of HS-25 or in Combination With Atorvastatin in Chinese Adults With Primary Hypercholesterolemia

HS-25-C-01
Start date: February 28, 2015
Phase: Phase 3
Study type: Interventional

To determine the efficacy of the HS-25 (10mg or 20mg) or in combination with Atorvastatin (10mg)in reducing low density lipoprotein-cholesterol (LDL-C) levels after a 12-week period of treatment in adults with primary hypercholesterolemia; To determine the safety of HS-25 (10mg or 20mg) or in combination with Atorvastatin (10mg)in subjects with LDL-C after a 40-week period of treament.

NCT ID: NCT03346733 Active, not recruiting - Clinical trials for Hypercholesterolemia

The Effect of Psyllium Fibre on LDL-C, Non-HDL-C, and Apolioprotein-B: A Systematic Review and Meta-analysis

Start date: October 8, 2013
Phase: N/A
Study type: Observational

Serum cholesterol is a major modifiable risk factor for cardiovascular disease, which despite considerable reduction in prevalence, remains the leading cause of premature mortality worldwide. Although LDL-C continues to be recognized as the primary therapeutic target, accumulating evidence suggests that alternative lipid parameters, non-HDL-C and apoB, may provide predictive value beyond that of LDL-C alone, in most population categories. Numerous lifestyle strategies have been developed to manage elevated cholesterol concentrations, of which viscous fibre is often encouraged for its beneficial effects on LDL-C reduction. Conversely, the effects of viscous fibre on new lipid markers, non-HDL and apoB, have yet to be defined. Therefore, this study seeks to elucidate the therapeutic potential of psyllium fibre on totality of atherogenic cholesterol and lipoprotein particles in a systematic review and meta-analysis of randomized controlled trials.

NCT ID: NCT03135184 Active, not recruiting - Clinical trials for Homozygous Familial Hypercholesterolemia

HDL Acute Lipid Optimization in Homozygous Familial Hypercholesterolemia

Start date: January 26, 2018
Phase: N/A
Study type: Interventional

Assess the effect on coronary atheroma of serial infusions of autologous selectively delipidated HDL/preβ enriched plasma following use of HDL Therapeutics PDS-2™ System