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Insulin Resistance clinical trials

View clinical trials related to Insulin Resistance.

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NCT ID: NCT04267705 Active, not recruiting - Clinical trials for Inflammatory Response

Pulses Consumption and Its Role in Managing Systemic Inflammation, Insulin Sensitivity and Gut Microbiome in Human

PS
Start date: February 24, 2020
Phase: N/A
Study type: Interventional

Objective 1: Characterize indices of systemic inflammation and gut microbiota composition and function after chronic (12 weeks) intake of pulses compared to control diet in human OW/OB-IR participants. Objective 2: Characterize dietary- and microbial-derived metabolite pools after regular intake of pulses (12 weeks) in human participants with OW/OB-IR compared to control diet. Objective 3: Characterize cognitive functioning after chronic (12 weeks) intake of pulses compared to control diet in human OW/OB-IR participants.

NCT ID: NCT04221152 Active, not recruiting - Clinical trials for Insulin Resistance Syndrome

A Extension Study of Empagliflozin in Patients With Refractory Diabetes Mellitus With Insulin Resistance ( EMPIRE-02 )

EMPIRE-02
Start date: February 1, 2020
Phase: Phase 3
Study type: Interventional

A multicenter, open-label, single-arm, extension study with regard to the safety and efficacy of empagliflozin in patients with refractory diabetes mellitus with insulin resistance.

NCT ID: NCT04167761 Active, not recruiting - Clinical trials for Cardiovascular Diseases

Ertugliflozin: Cardioprotective Effects on Epicardial Fat

Start date: July 1, 2020
Phase: Early Phase 1
Study type: Interventional

The purpose of this study is to learn if Sodium-Glucose Cotransporter 2 inhibitor (SGLT2i) medications enhance beneficial properties of epicardial adipose tissue including metabolic flexibility, insulin sensitivity, decreased cell size and reduced inflammation.

NCT ID: NCT04067752 Active, not recruiting - Clinical trials for End-stage Renal Disease

Nutrition, Inflammation and Insulin Resistance in End-Stage Renal Disease

SummerMRI
Start date: March 1, 2022
Phase: N/A
Study type: Interventional

By 2030 an estimated 2 million people in the US will need dialysis or transplantation. Insulin resistance and chronic inflammation are common in dialysis patients and have been linked to protein-energy wasting, the most important determinant of clinical outcome in this patient population. The investigators hypothesize that the skin and muscle tissue sodium accumulation is a critical mechanism by which chronic inflammatory response and insulin resistance, alone or in combination lead to protein energy wasting in hemodialysis patients. The investigators will test this hypothesis by studying dialysis patients and matched controls without kidney disease by examining tissue Na content, markers of inflammation and protein metabolism.

NCT ID: NCT04028921 Active, not recruiting - Obesity Clinical Trials

Activity, Adiposity, and Appetite in Adolescents 2

AAAA2
Start date: January 3, 2022
Phase:
Study type: Observational

Our goal is to examine linkages between physical activity, appetite control, and energy metabolism in adolescents. The investigators will assess metabolic function and appetite control in male and female adolescents stratified by bodyweight and physical activity using across-sectional study design.

NCT ID: NCT04027712 Active, not recruiting - Diabetes Clinical Trials

Platelet Reactivity, B-amyloid, MOTS-c and Mortality of Type II Diabetics With CAD

Start date: January 1, 2014
Phase:
Study type: Observational

Increased circulating b-amyloid and decreased Mitochondrial-derived peptide (MOTS-c), a peptide improving tissue insulin sensitivity, are reported in diabetes. The investigators plan to investigate the association of both biofactors with high on-clopidogrel platelet reactivity and cardiovascular mortality in type 2 diabetic patients with Coronary artery disease

NCT ID: NCT04018365 Active, not recruiting - Clinical trials for Insulin Resistance Syndrome

A Study of Empagliflozin in Patients With Refractory Diabetes Mellitus With Insulin Resistance

EMPIRE-01
Start date: September 1, 2019
Phase: Phase 3
Study type: Interventional

A multicenter, open-label, single-arm study with regard to the efficacy and safety of empagliflozin in patients with refractory diabetes mellitus with insulin resistance

NCT ID: NCT04011618 Active, not recruiting - Metabolic Syndrome Clinical Trials

Effect of Ellagic Ácid on the Components of Metabolic Syndrome, Insulin Sensitivity and Insulin Secretion

Start date: September 17, 2019
Phase: Phase 2
Study type: Interventional

Metabolic syndrome (MetS) is a group of important cardiovascular risk factors: abdominal obesity, dyslipidemia, hyperglycemia, and high blood pressure. Treatment requires lifestyle changes and pharmacological therapy with different medications for each component. Ellagic acid (EA) is a polyphenol that has shown health benefits in multiple experimental studies. Patients consume EA without prescription; considering there aren't studies that demonstrate its effectiveness on MetS, it is important to evaluate the possible effects of AE on this pathology. METHODOLOGY: Current study is a double-blind, placebo-controlled clinical trial. The aim of this study is to evaluate the effect of AE on the components of metabolic syndrome, insulin sensitivity, and insulin secretion.

NCT ID: NCT03960333 Active, not recruiting - Obesity Clinical Trials

Immunometabolism in Pediatric Obesity

IPO
Start date: April 25, 2019
Phase:
Study type: Observational

This is a study to learn about obesity and how insulin resistance and Type 2 Diabetes develops in children.

NCT ID: NCT03854981 Active, not recruiting - Clinical trials for Bariatric Surgery Candidate

Pre-operative Exercise and Nutrition Therapy on Cardio-metabolic Health in Patients Undergoing Bariatric Surgery

Start date: August 11, 2015
Phase: N/A
Study type: Interventional

Obesity is a major health concern that has been associated with an estimated 2.8 million deaths worldwide each year. The number of individuals considered obese with a Body Mass Index (BMI) above 30 kg/m2 has grown to more than 500 million. The increased morbidity and mortality associated with obesity stems from a long list of comorbidities, including hypertension, coronary artery disease, stroke, cancer, and type 2 diabetes (T2D). Bariatric surgery is an emerging intervention that has been used frequently to induce weight loss for obese individuals and it has been shown to improve glycemic control and insulin resistance in people at risk for type 2 diabetes. Surgery may also lead to healthy improvements in inflammation, immune cells and vascular health. It is already known that exercise and weight loss from lifestyle modification can improve glycemic control, insulin resistance, inflammation, and arterial stiffness. However, no work has been done to examine a combination of bariatric surgery and pre-surgery exercise. Recent work by the team has evidence demonstrating that health status pre-surgery has an impact on post-surgery outcomes. Such findings suggest that improvements in health status from exercise before surgery may improve surgery outcomes as well as surgery-induced health outcomes. To date, no study has systematically examined the role of exercise on the prevalence of surgery complications or on post-surgery weight loss, glycemic control, and insulin resistance. Moreover, no work currently exists on exercise, with or without bariatric surgery on adipose tissue derived inflammation. Therefore, the purpose of this study is to investigate the effect of pre-surgery lifestyle intervention with exercise on bariatric surgery outcomes. To test this objective, subjects will participate in a match paired study, based on BMI. Subjects will undergo testing of blood chemistry and related measures of health before (pre-test) and after (post) intervention. Then all subjects will receive bariatric surgery. Post surgery outcomes will be assessed by examining surgery operating time, changes in blood chemistry, adipose tissue biopsies and other measures indicative of glucose and vascular health. After this surgery, subjects will return for testing about 30d later.