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Hyperlipoproteinemias clinical trials

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NCT ID: NCT02577159 Active, not recruiting - Clinical trials for Diabetes Mellitus, Type 2

Dapagliflozin on Hyperlipidemia and Insulin Resistance in Type 2 Diabetic Patients (DAPHNIS Study)

DAPHNIS
Start date: July 1, 2015
Phase: Phase 4
Study type: Interventional

The investigators will investigate whether dapagliflozin (FORXIGA) might improve lipoprotein metabolism as well as hyperglycemia in Japanese patients with type II diabetes mellitus whose HbA1c levels are less than 7.0% (from 20 to 65 years of age). The investigators will examine changes of fasting lipoprotein profile including TG, TC, HDL-C, apoB-48 and RemL-C before and after the 8 weeks administration of dapagliflozin.

NCT ID: NCT02512276 Completed - Hypertension Clinical Trials

Tele-Pharmacy Intervention to Improve Treatment Adherence

STIC2IT
Start date: August 2015
Phase: N/A
Study type: Interventional

The purpose of this cluster randomized controlled trial is to evaluate whether a novel tele-pharmacist-based intervention for patients with hyperlipidemia, hypertension, and diabetes improves medication adherence, disease control, and patients' understanding of their treatment.

NCT ID: NCT02506920 Completed - Hyperlipidemia Clinical Trials

Gender Dependent Difference in Lipemia After 6 x OFTT in Young Healthy Subjects

Start date: January 1997
Phase: N/A
Study type: Interventional

The investigators wanted to study the postprandial lipemia after six oral fat tolerance test with varying amounts of saturated fat in young healthy subjects.

NCT ID: NCT02458287 Completed - Hyperlipidemia Clinical Trials

Efficacy, Safety, Tolerability And Actual Use Study Of Bococizumab And An Autoinjector (Pre-Filled Pen) In Subjects With Hyperlipidemia Or Dyslipidemia

SPIRE-AI
Start date: June 2015
Phase: Phase 3
Study type: Interventional

This study is a multicenter, randomized study in subjects with high cholesterol receiving statins to assess the efficacy to lower LDL-C, the safety, tolerability and actual use of bococizumab and an autoinjector (pre-filled pen).

NCT ID: NCT02449187 Completed - Diabetes Clinical Trials

Investigate the Effect of Food on the Pharmacokinetics of JLP-1310 in Healthy Male Volunteers

Start date: August 2, 2017
Phase: Phase 1
Study type: Interventional

A randomized, open-label, single dose, crossover study to investigate the effect of food on the pharmacokinetics of JLP-1310 in healthy male volunteers.

NCT ID: NCT02433288 Completed - Dyslipidemia Clinical Trials

Rosuvastatin Adherence App Study in China

eHELP China
Start date: July 20, 2015
Phase: N/A
Study type: Interventional

This is a randomized, two-arm, open label, Phase IV clinical trial to evaluate if the provision of a smart phone-based patient support tool prolongs the patient's rosuvastatin treatment duration.

NCT ID: NCT02428998 Completed - Healthy Clinical Trials

Safety for 24 Weeks Intake of Korean Red Ginseng in Adults

Start date: September 2014
Phase: N/A
Study type: Interventional

Korean Red Ginseng appears to adverse events in adults taking 24 weeks Placebo and comparative assessment. And exploratory as Korean Red Ginseng blood sugar control, reduce body fat, URTI prevention, cardiovascular risk, renal function, cholesterol, improve, fatigue, and determine the impact on biological age.

NCT ID: NCT02298894 Unknown status - Hyperlipidemia Clinical Trials

Comparison of LDL Particle Count With Other Available Lipid Tests

LIPID
Start date: November 2014
Phase: N/A
Study type: Observational

Despite the wide availability of advanced lipoprotein tests, no reference standard exists for Low Density Lipoprotein Cholesterol (LDL-C) due to inherent problems with each of the assays. Newer methods for estimating LDL particle numbers, including nuclear magnetic resonance (NMR) spectroscopy and vertical auto profile (VAP) are currently under investigation. NMR has been proposed as having the best correlation with adverse cardiovascular outcomes. Unfortunately, the accuracy of LDL-C or LDL particle number measurements is currently not monitored by national standardization programs. Direct comparisons between the various testing methods have been limited restricting our ability to accurately interpret and compare values across vendors and lipid parameters. Our hypothesis is that: 1. LDL particle count numbers, as determined by NMR (Liposcience), provides the best estimates of cardiovascular risk. 2. Discrepancies exist between the LDL particle count by NMR and other values as presented by calculated LDLC and directly measured LDL (VAP and ion mobility). The investigators will enroll 100 patients recruited from the Lipid Clinic at the Scripps Center for Integrative Medicine. Each patient will have one blood draw from which four tests will be analyzed. Risks are associated with drawing blood, which will be minimized by using Scripps Clinic Lab technicians. The potential loss of personal health information will be reduced by limiting access to study and lab staff and keeping information password-protected on Scripps servers.

NCT ID: NCT02227784 Terminated - Hyperlipidemia Clinical Trials

A Study of Evacetrapib (LY2484595) in Participants With High Cholesterol

ACCENTUATE
Start date: October 2014
Phase: Phase 3
Study type: Interventional

The purpose of the ACCENTUATE study is to evaluate whether the study drug known as evacetrapib is effective in treating participants with high cholesterol and atherosclerotic cardiovascular disease (ASCVD) and/or diabetes.

NCT ID: NCT02215408 Completed - Hypertension Clinical Trials

MEDication Focused Outpatient Care for Underutilization of Secondary Prevention

MEDFOCUS
Start date: January 20, 2015
Phase: N/A
Study type: Interventional

The study tested whether a pharmacist-run cardiovascular risk service (CVRS) at the University of Iowa can increase use of national standards of care in clinics