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Hyperlipidemias clinical trials

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NCT ID: NCT05767996 Enrolling by invitation - Clinical trials for Familial Hyperlipidemia

School-based Education and Screening Program With Lipid Screening as a Means to Identify Familial Hyperlipidemia

Start date: February 1, 2023
Phase:
Study type: Observational

Determination of FH status by genetic testing in school age children who have demonstrated elevated cholesterol on baseline screening.

NCT ID: NCT05742022 Completed - Clinical trials for Combined Hyperlipidemia

"Phospholipovit" vs Placebo in Patients With Combined Hyperlipidemia

Start date: January 1, 2016
Phase: Phase 2/Phase 3
Study type: Interventional

"Phospholipovit" vs placebo in patients with combined hyperlipidemia

NCT ID: NCT05737355 Not yet recruiting - Hyperlipidemias Clinical Trials

Effect of ANKASCIN 568-P Products Regulating Blood Lipid

Start date: April 1, 2023
Phase: N/A
Study type: Interventional

This study is a randomized, double-blind, placebo-controlled, parallel-controlled trial (24 weeks in total), divided into three periods (screening, treatment, and discontinuation follow-up)

NCT ID: NCT05729659 Completed - Oxidative Stress Clinical Trials

Sideritis Supplementation, Oxidative Stress and Health

Start date: February 15, 2023
Phase: N/A
Study type: Interventional

The aim of the present clinical study is to estimate the efficacy of a Sideritis Scardica extract (SidTea+), derived from the Greek mountain Taygetos, in regulating antioxidant and health biomarkers in healthy adults.

NCT ID: NCT05720156 Recruiting - Stroke Clinical Trials

Immunomodulatory Effects of PCSK9 Inhibition

INSPIRAR
Start date: April 4, 2024
Phase:
Study type: Observational

Cardiovascular disease (CVD) represents the leading cause of death worldwide. While medications, such as statins, significantly reduce atherosclerotic CVD (ASCVD) risk by lowering low density lipoprotein levels, they may also have pleiotropic effects on inflammation. The immunomodulatory effects of these medications are relevant to ASCVD risk reduction given that inflammation plays a central role in atherosclerotic plaque formation (atherogenesis) and influences the development of vulnerable plaque morphology. Patients on statins, however, may have residual inflammation contributing to incident ASCVD despite the potent LDL-lowering effects of statins. While new therapies, such as proprotein convertase subtilisin/kexin type 9 (PSCK9) inhibitors, further reduce incident ASCVD and drastically reduce LDL-C below that achieved by statin therapy alone, PCSK9 inhibitors may also have pleiotropic effects on inflammation. Thus, PCSK9 inhibitors may help reduce arterial inflammation to a level closer to that of patients without ASCVD. This study will apply a novel targeted molecular imaging approach, technetium 99m (99mTc)-tilmanocept SPECT/CT, to determine if residual macrophage-specific arterial inflammation is present with statin therapy and the immunomodulatory effects of PSCK9 inhibition. Given the continued high mortality and morbidity attributable to ASCVD, strong imperatives exist to better understand the immunomodulatory effects of lipid lowering therapies and residual inflammatory risk. This understanding, in turn, will inform the development of new ASCVD preventative and treatment strategies as well as elucidate other indications for established therapies.

NCT ID: NCT05712070 Not yet recruiting - Hypertension Clinical Trials

Mobile Application for Cardiovascular Risk Treatment

iSMART-CV
Start date: March 2, 2023
Phase: N/A
Study type: Interventional

This study is a randomized, open-label clinical trial to validate the efficacy and safety of smartphone app-guided life style modification for the management of hypertension and hyperlipidemia.

NCT ID: NCT05704439 Not yet recruiting - Hypertension Clinical Trials

Cardiovascular Risk Reduction in Epilepsy

Start date: January 2024
Phase: N/A
Study type: Interventional

Epilepsy is a disabling and lethal neurological disease which affect 3.47 million Americans. Significant health care disparities exist in people with epilepsy (PWE). Hypertension and hyperlipidemia are highly prevalent and often go undertreated, and cardiovascular (CV) mortality is higher in people with epilepsy (PWE) than the general population. Preliminary data from our group shows that PWE have higher ACC-ASCVD risk scores than an age matched NHANES cohort without epilepsy. Preliminary data also demonstrate mortality rates in PWE due to hypertension, stroke, and diabetes are rising in the US, counter to the US general population. This proposal seeks to test the feasibility, acceptability, and preliminary efficacy of a new care model for the underserved PWE in a public health setting. In this new model, neurologists guided by standardized treatment algorithms (ACC-ASCVD estimator+) propose and initiate pharmacological interventions for hypertension and hyperlipidemia.

NCT ID: NCT05703386 Recruiting - Hypertension Clinical Trials

Imaging the Pathogenesis of Cerebral Small Vessel Disease

Start date: November 8, 2022
Phase:
Study type: Observational

Cerebral small vessel disease (CSVD) can lead to vascular cognitive impairment and dementia (VCID). The hallmark of CSVD is the appearance and progression of white matter hyperintensities (WMH) on MRI. The goal of this study it to recruit and follow individuals at risk for WMH progression and use serial MRI scanning to gain insights into the pathogenesis of CSVD.

NCT ID: NCT05703282 Recruiting - Hyperlipidemias Clinical Trials

A Study to Assess the Safety and Pharmacokinetics of AD-104-A

Start date: March 13, 2023
Phase: Phase 1
Study type: Interventional

Primary endpoint of this study is to evaluate the pharmacokinetic characteristics of AD-104-A

NCT ID: NCT05681247 Completed - Hyperlipidemias Clinical Trials

Bioavailability and Bioequivalence of Ezetimibe Tablets in Healthy Subjects

Start date: December 17, 2017
Phase: Phase 1
Study type: Interventional

This study was conducted to assess the bioequivalence of the ezetimibe tablet to Ezetrol ® in healthy Chinese volunteers and estimate the pharmacokinetic proļ¬les of ezetimibe tablet.