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Prediabetic State clinical trials

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NCT ID: NCT04234217 Recruiting - Sleep Apnea Clinical Trials

Mechanisms of Prediabetic States in Sleep Apnea

Start date: November 26, 2019
Phase: N/A
Study type: Interventional

The purpose of this study is to better understand how sleep apnea contributes to the development of diabetes.

NCT ID: NCT04225507 Recruiting - PreDiabetes Clinical Trials

Technology-Supported Treatment of Sleep Apnea in Prediabetes

TECH
Start date: April 13, 2021
Phase: N/A
Study type: Interventional

Despite the efficacy of intensive lifestyle interventions in prediabetes, the incidence of diabetes is rising, and thus there is a critical need for additional strategies to prevent diabetes and to reduce its cardiovascular complications in this high-risk population. Sleep apnea is a highly common condition in prediabetes, but it has been mostly ignored and undertreated in current practice. The proposed study will be the first to assess whether adding CPAP (continuous positive air pressure) treatment to a lifestyle intervention improves cardiometabolic outcomes beyond that achieved with lifestyle alone (i.e. current standard of care) in high-risk individuals with prediabetes.

NCT ID: NCT04210128 Completed - Breast Cancer Clinical Trials

Glucose Monitoring to Predict and Treat High Glucose Levels After Steroid Treatment

Start date: December 20, 2019
Phase:
Study type: Observational

The purpose of this study is to see if continuous glucose monitoring can identify how often people who have pre-diabetes or medical obesity or well-controlled diabetes experience very high glucose values while receiving chemotherapy for breast cancer or pancreatic.

NCT ID: NCT04201600 Recruiting - Depression Clinical Trials

Glucose Variability and Cognition in Prediabetes

Start date: March 1, 2022
Phase:
Study type: Observational

This study examines the association of variability in glucose values over a 10-day period with cognitive function and functional status among individuals with prediabetes, aged 50 or older.

NCT ID: NCT04168372 Recruiting - Insulin Resistance Clinical Trials

Fructose: Substrate, Stimulus, or Both?

Start date: September 15, 2019
Phase: N/A
Study type: Interventional

This objective of this study is to use sensitive methodology under controlled conditions to investigate the mechanisms by which fructose consumption contributes to excess fatty acid synthesis and elevations in blood glucose levels following consumption of meals containing fructose.

NCT ID: NCT04150926 Completed - Prediabetic State Clinical Trials

The Effect of Black Currant on Postprandial Glucose Metabolism

MAQUA
Start date: August 15, 2019
Phase: N/A
Study type: Interventional

The study examines the effect of black currant on glucose and insulin concentrations after a meal. In addition, the cytokine and free fatty acids levels are of interest.

NCT ID: NCT04144920 Completed - Pre Diabetes Clinical Trials

Evaluating the Acute Glycemic Response to Different Strategies of Breaking Up Sedentary Time

Start date: August 1, 2018
Phase: N/A
Study type: Interventional

This study aims to determine the most effective strategy of reducing sedentary behavior to improve health. Specifically, we aim to answer the following questions: (a) To determine if there is a significant difference in acute post-prandial glucose response between continuous sitting and two intermittent standing regimes (high frequency, low duration breaks (HFLD) and low frequency, high duration breaks (LFHD)). We hypothesize that intermittent standing (combined HFLD breaks and LFHD breaks regimes) will result in lower overall acute post-prandial glucose compared to continuous sitting. (b) To determine if there is a significant difference in acute post-prandial glucose response between two strategies to reduce sitting with standing (HFLD standing breaks vs. LFHD standing breaks). We hypothesize that the HFLD breaks condition will elicit lower acute post-prandial glucose level compared to the LFHD breaks condition. All eligible participants will be consented and subjected to all three study conditions: (i) Uninterrupted sitting, (ii) HFLD breaks, and (iii) LFHD breaks. The order at which participants were subjected to these conditions will be randomly determined and each condition were performed a week apart. Standardized meals (breakfast and lunch) will be provided during each lab visit and participants will be then be asked to perform their usual work activity using a sit-stand workstation in the lab. Depending on their assigned condition, the participants will be prompted to stand or sit for a given period of time. A continuous glucose monitor will be used to measure glucose response to the intervention while an activPAL device will be used to make sure that participants are compliant with the study protocol.

NCT ID: NCT04134650 Recruiting - Insulin Resistance Clinical Trials

Effect of Low Dose Combination of Linagliptin + Metformin to Prevent Diabetes

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

Type 2 diabetes is a chronic disease that has reached global epidemic proportions due to the growing number of patients in all countries; It has become the disease that causes more chronic and acute complications to patients, unfortunately, when the diagnosis of type 2 diabetes is made patients are identified at very advanced stages of the disease. For all the above, the best strategies will be those that are aimed at early stages of the disease, and the investigators are convinced that the use the combination of drugs with additive pathophysiological effect plus cardiovascular protection in early stages, will have better results, lasting and with greater results impact on the natural history of the disease that throws measures that may have an applicability in clinical practice, in order to contribute to the control of this pathology. Therefore, the combination of medications with different mechanisms of action, in low doses, could be a useful strategy not only to prevent type 2 diabetes, but also to prevent macro and microvascular complications early. The goal of this clinical trial is to evaluate the effect of low doses of linagliptin + metformin vs metformin alone on physiopathological parameters, such as glucose metabolism, insulin resistance, insulin secretion and pancreatic beta cell function in patients with impaired fasting glucose plus impaired glucose tolerance, during 12 months.

NCT ID: NCT04132908 Completed - PreDiabetes Clinical Trials

Clinical Trial to Evaluate the Effect of an Extract of Sclerocaya Birrea on Prediabetic Subjects

PRED
Start date: October 1, 2016
Phase: N/A
Study type: Interventional

It consists in the intake, during a period of 10 weeks, of a nutraceutical (natural extract of Sclerocarya birrea). It is a clinical trial, during which certain parameters of the glucidic metabolism will be measured analytically. Other secondary variables such as lipid profile, inflammatory markers, blood pressure, endothelial function and body composition will also be determined.

NCT ID: NCT04131582 Recruiting - Insulin Resistance Clinical Trials

Effect of Empagliflozin + Linagliptin + Metformin + Lifestyle in Patients With Prediabetes

4T
Start date: September 1, 2019
Phase: Phase 3
Study type: Interventional

Type 2 diabetes is a worldwide epidemic disease, and preventive strategies are needed to face this health problem. The goal of this trial is to evaluate the effect of empagliflozin + linagliptin + metformin + lifestyle on physiopathological parameters, sush as glucose metabolism, insulin resistance, pancreatic beta cell function and cardiovascular function in patients with impaired fasting glucose plus impaired glucose tolerance, during 12 months