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Hyperglycemia clinical trials

View clinical trials related to Hyperglycemia.

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NCT ID: NCT03076775 Completed - Clinical trials for Neonatal Hypoglycemia

Euglycemia After Antenatal Late Preterm Steroids, the E-ALPS Study

E-ALPS
Start date: June 8, 2017
Phase: N/A
Study type: Interventional

Annually in the U.S 300,000 neonates are born late preterm, defined as 34 weeks 0 days - 36 weeks 6 days. The Antenatal Late Preterm Steroids (ALPS) Trial demonstrated that maternal treatment with betamethasone in the late preterm period significantly reduces neonatal respiratory complications, but also increases neonatal hypoglycemia, compared to placebo. This research study will attempt to answer the following primary question: Does a management protocol aimed at maintaining maternal euglycemia after ALPS decrease fetal hyperinsulinemia, compared to usual antepartum care?

NCT ID: NCT03055169 Completed - Hyperglycemia Clinical Trials

TCF7L2 Polymorphisms Influence on Glycemic Control in ICU Patients With Organ Failure

READIAB-G4
Start date: April 2012
Phase:
Study type: Observational

This study evaluates the link between genetic polymorphisms as r7903146, rs12255372 of TCF7L2 gene and the risk of developing hyperglycemia during Intensive care unit stay

NCT ID: NCT03047824 Completed - Clinical trials for Metabolic Stress Hyperglycemia

Effects of GlucoClear CGM System on the Performance of Insulin Therapy in Critically Ill Patients

GlucoClearIT
Start date: May 2014
Phase: N/A
Study type: Interventional

After providing written informed consent, the first 20 Subjects meeting Inclusion/Exclusion Criteria will be consecutively enrolled in the Standard of Care cohort. The moderate treatment cohort will then be consecutively enrolled, followed by the tight glycemic control cohort. After sensor insertion, baseline evaluations including APACHE II, SOFA, and laboratory evaluations will be determined. Subjects enrolled in the standard of care cohort will be treated according to the institution's protocol for measuring glucose and managing insulin. These subjects will be monitored on a GlucoClear System but they will not be managed based on the values or trends of the GlucoClear system. Subjects enrolled in the treatment cohorts will be monitored and managed with a special version of the GlucoClear continuous monitoring system. This system contains the GlucoClear Insulin Dosing Algorithm providing insulin dosing recommendations to enable the clinician to manage patient glucose within pre-specified target levels. These recommendations are presented on screen for a clinical professional to approve or override. Subjects in the moderate treatment cohort will have their glucose managed in the range of 120 - 180 mg/dl. Subjects in the tight glycemic control treatment cohort will be managed in the range of 80 - 120 mg/dl. After discharge from the ICU, subjects will followed for adverse events and mortality at 30 days, either by telephone contact or office visit.

NCT ID: NCT03027570 Completed - Body Image Clinical Trials

The Impact of Incorporating an Exergame Activity Application in a Treatment Regimen for Overweight Children

Start date: March 2, 2017
Phase: N/A
Study type: Interventional

80 children aged 5-13, BMI≥85%, will be recruited to a program for the treatment of overweight children.The intervention group will use the app "Just Dance Now" and The control group will be exposed to the usual program without the app. Measurements will be performed at the beginning of the program, the end and 3 months after completion of the intervention.

NCT ID: NCT03023228 Completed - Diabetes Mellitus Clinical Trials

Diabetes To Go: An Inpatient Diabetes Survival Skills Education Program

Start date: May 2010
Phase: N/A
Study type: Interventional

A learner-centered diabetes survival skills self-management education program was provided to adults with uncontrolled diabetes in the hospital and generated preliminary evidence of impact on medication adherence and a trend toward reduction in hospital and emergency department admissions.

NCT ID: NCT03018600 Completed - Clinical trials for Glucocorticoid-induced Hyperglycemia

Continuous Glucose Monitoring on Patients With Active Autoimmune Diseases Following High-dose Predisone Treatment

CGM
Start date: January 2016
Phase: N/A
Study type: Observational

Glucocorticoid is widely used in clinical treatment. Recently, there was research about glucose fluctuations under low-dose and pulse steroid therapy in elderly patients with active autoimmune diseases. Through this prospective trial, the investigators wanted to know the blood glucose characteristics under high dosage glucocorticoid (1-2 mg/kg/day prednisone or equivalent) in young patients (30-40 years) with active autoimmune diseases with or without low-dose glucocorticoid maintenance. The investigators used continuous glucose monitoring for 72 hours to get a better understanding of the glucose levels.

NCT ID: NCT03012867 Completed - Clinical trials for Hyperglycemia Stress

Enteral Nutrition and Glucose Homeostasis

Start date: June 2010
Phase: Phase 4
Study type: Interventional

Different enteral nutrition formulas are tested on their effect on glucose homeostasis in critically ill medical patients.

NCT ID: NCT02999386 Completed - Diabetes Mellitus Clinical Trials

Stress Induced Hyperglycemia In Trauma

SIHG
Start date: October 2016
Phase:
Study type: Observational

The clinical relevance of the observed stress induced hyperglycemia in trauma patients remains unclear. The earlier studies suggested the implications of cytokines in stress induced hyperglycemia and the outcomes after trauma. To date, there is little information available regarding the effect of diabetic hyperglycemia (occult or known) on outcomes after trauma and whether these patients represent a distinct group with differential outcomes when compared to those with stress-induced hyperglycemia. Herein, the purpose of this study is to identify the incidence of stress induced hyperglycemia as well as diabetic hyperglycemia in trauma patients and to investigate the association between proinflammatory cytokine levels and hyperglycemia in our trauma population.

NCT ID: NCT02971202 Completed - Insulin Resistance Clinical Trials

Contribution of Hyperinsulinemia vs. Hyperglycemia to Insulin Resistance in Type 1 Diabetes and Maturity Onset Diabetes of the Young, Type 2 (MODY2)

Start date: December 2016
Phase: Phase 1
Study type: Interventional

The purpose of this study is to determine the key factors influencing insulin sensitivity in type 1 diabetes (T1DM) and maturity onset diabetes of the young, type 2 (MODY2). Our study tests the hypothesis that decreased insulin sensitivity is primarily driven by chronically elevated insulin levels in the blood rather than chronic elevations in blood sugar.

NCT ID: NCT02940249 Completed - Clinical trials for Prevention of Hyperglycaemia

Effects of an Apple Extract on Glycaemia: The GLU-Pomme Study

GLU-Pomme
Start date: January 2017
Phase: N/A
Study type: Interventional

Postprandial hyperglycaemia can lead to adverse modifications to functional proteins within the body and eventually lead to the development of type 2 diabetes. Previous research by this group has shown that an apple polyphenol extract reduced hyperglycaemia following a high-carbohydrate meal. The aim of this study is to investigate the effects of lower doses of the apple extract on postprandial glycaemia, insulinaemia and plasma gastric inhibitory polypeptide concentrations following a mixed carbohydrate test meal.