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Hypercholesterolemia clinical trials

View clinical trials related to Hypercholesterolemia.

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NCT ID: NCT04677335 Completed - Clinical trials for Hypercholesterolemia

Combination of AB-LIFE Probiotic Plus Monacolin K to Reduce Blood Cholesterol

Start date: October 1, 2014
Phase: N/A
Study type: Interventional

This randomized study evaluates the effectiveness of a nutraceutical combining billion colony forming units (cfu) of three L. plantarum strains (CECT7527, CECT7528 and CECT7529) and 10 mg of monacolin K in reducing blood cholesterol.

NCT ID: NCT04673721 Completed - Obesity Clinical Trials

PROSPective Evaluation of Fortified Eggs Related to Improvement in The Biomarker Profile for Your Health

PROSPERITY
Start date: January 6, 2021
Phase: N/A
Study type: Interventional

The objective of the study is to assess the effect of fortified eggs (compared to a non-egg supplemented diet) and intermittent fasting (IF) (compared to a usual care diet) on biomarker profile at 4 months. This will be a 140-participant, 2x2 factorial, randomized clinical trial comparing fortified eggs vs. a non-egg supplemented diet and IF vs. usual care diet through 4 months. Participants will be randomized 1:1:1:1 to the four treatment groups. Participants will have in-person follow-up visits at 1- and 4- months (inclusive of laboratory assessments) in addition to telephone calls at months 2 and 3. A subset of patients (~24 in each egg randomized strata) will undergo microbiome assessment at baseline and at 4 months.

NCT ID: NCT04669041 Completed - Clinical trials for Hypercholesterolemia

A Study to Evaluate the Efficacy and the Safety of Single Pill Combination (SPC) Ezetimibe/Rosuvastatin in Chinese Adult Patients With Primary Hypercholesterolemia Not Adequately Controlled on Statin Therapy

ROZEL
Start date: December 8, 2020
Phase: Phase 3
Study type: Interventional

Primary Objective: To demonstrate the superiority of the single pill combination (SPC) ezetimibe 10 mg/rosuvastatin 10 mg (E10/R10) compared to rosuvastatin 10 mg (R10), in the reduction of low density lipoprotein cholesterol (LDL-C) after 8 weeks. Secondary Objectives: - To evaluate the proportion of patients who attain their LDL-C goal. - To evaluate the effect of SPC (E10/R10) compared to rosuvastatin 10 mg (R10) in reduction of LDL-C at Week 4. - To evaluate the effect of SPC (E10/R10) compared to R10 on other lipid parameters at Week 4 and Week 8. - To evaluate the safety of SPC (E10/R10) and R10.

NCT ID: NCT04666298 Completed - Clinical trials for Hypercholesterolemia

Study of Efficacy and Safety of Inclisiran in Japanese Participants With High Cardiovascular Risk and Elevated LDL-C

ORION-15
Start date: January 29, 2021
Phase: Phase 2
Study type: Interventional

This was a placebo-controlled, double-blind, randomized trial in Japanese participants with history of coronary artery disease (CAD) or participants categorized in 'high risk' by JAS 2017 guideline, or Japanese participants with heterozygous familial hypercholesterolemia (HeFH) and elevated Low-density lipoprotein cholesterol (LDL-C) despite maximum tolerated dose of statin(s) to evaluate the efficacy, safety, tolerability, and PK of subcutaneous inclisiran injection(s).

NCT ID: NCT04652349 Completed - Clinical trials for Primary Hypercholesterolemia

Efficacy and Safety of HGP1910 and HCP1903 in Patients With Primary Hypercholesterolemia

Start date: July 6, 2020
Phase: Phase 3
Study type: Interventional

The purpose of this study is to investigate the safety and clinical efficacy of HGP1910 and HCP1903 in patients with primary hypercholesterolemia

NCT ID: NCT04643093 Completed - Clinical trials for Primary Hypercholesterolemia

Compare the Efficacy and Safety of 1PC111 With Pitavastatin and Ezetimibe in Patients With Primary Hypercholesterolemia or Mixed Dyslipidemia

Start date: August 1, 2020
Phase: Phase 3
Study type: Interventional

The study is to evaluate whether the efficacy of 1PC111 is superior to pitavastatin and ezetimibe in patients with primary hypercholesterolemia or mixed dyslipidemia in the 12 week treatment period.

NCT ID: NCT04596358 Completed - Hypertension Clinical Trials

Interplay Between Adherence to the Mediterranean Diet, Lipid Profile and Blood Pressure: a Comparative Survey Among Healthcare and Non-Healthcare Female Workers

Start date: March 10, 2018
Phase:
Study type: Observational

The study aims at testing the level of adherence to the Mediterranean diet among health-workers, comparing this aspect to the extra-working physical activity, anthropometric measures and prevalence of cardiovascular, metabolic and neoplastic diseases previously diagnosed.

NCT ID: NCT04584736 Completed - Clinical trials for Primary Hypercholesterolemia

To Evaluate the Efficacy and Safety in Patients With Primary Hypercholesterolemia

Start date: June 11, 2019
Phase: Phase 3
Study type: Interventional

To Evaluate the Efficacy and Safety of Combination Therapy of Pitavastatin and Ezetimibe Versus Monotherapy of Pitavastatin in Patients With Primary Hypercholesterolemia.

NCT ID: NCT04574505 Completed - Clinical trials for Hypercholesterolemia

Food Supplementation With Eufortyn Colesterolo Plus for LDL Modulation in Subjects With Polygenic Hypercholesterolemia

ANEMONE
Start date: September 14, 2020
Phase: N/A
Study type: Interventional

This is a two-arm randomized, placebo-controlled, double-blind, monocentric parallel-groups clinical study conducted in Italy. The objective of this study is to evaluate the effect of dietary supplementation of a combined supplement containing bergamot (Vazguard®) phytosomal polyphenolic fraction associated with standardized artichoke extract (Pycrinil®, Cynara cardunculus) and Cynara scolimus, associated with high coenzyme Q10 bioavailability (Q10 phytosome® Ubiqsome) and zinc, on the glycometabolic structure of subjects with suboptimal levels of LDL cholesterolemia compared with placebo.

NCT ID: NCT04573218 Completed - Clinical trials for Hypercholesterolemia

Supplementation of Oil Palm Phenolics to Improve Lipid Profile in Subjects With Minor Hyperlipidaemia

Start date: October 18, 2021
Phase: Phase 2
Study type: Interventional

An unpublished study by the investigators on healthy participants has shown that the supplementation of oil palm phenolics (OPP) at 250 mg is the optimum dose to demonstrate the ability to lower total and LDL cholesterol. There is no clinical evidence as yet on that optimum dosage of OPP supplementation in improving fasting lipid profile in minor hyperlipidemia subjects. The investigators hypothesize that in a clinical study, OPP supplemented to the minor hyperlipidemic participants will elicit a reduction in total and LDL cholesterol while maintaining safety and tolerability. OPP may have the potential to be positioned as natural health supplement in improving lipid profile.