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Hyperglycemia clinical trials

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NCT ID: NCT02574156 Terminated - Hyperglycemia Clinical Trials

Control of Hyperglycemia After Cardiac Surgery: CHyCS Trial

CHyCS
Start date: January 1, 2017
Phase: Phase 3
Study type: Interventional

The investigators aim to study the impact of a strategy of a intensive glycemic control in patients undergoing cardiac surgery.

NCT ID: NCT02303405 Terminated - Clinical trials for Diabetes Mellitus Type 2 With Hyperglycemia

Hydroxychloroquine Versus Pioglitazone in Combination Treatment for Type 2 Diabetes Mellitus

Start date: November 2014
Phase: Phase 2
Study type: Interventional

A 4-month, randomized, prospective, open-label comparison trial of hydroxychloroquine vs. pioglitazone in type 2 diabetic patients inadequately controlled on maximally tolerated doses of metformin plus a sulfonylurea.

NCT ID: NCT02068989 Terminated - Clinical trials for Diabetes Mellitus Type 2

Study of Stress Hyperglycemia as an Indicator of Diabetes Mellitus

Start date: February 2013
Phase: N/A
Study type: Observational

We hypothesize that stress hyperglycemia is an indicator that a patient will develop type 2 diabetes mellitus in the future. Subjects who are not diabetic are enrolled and blood glucose readings reviewed during their intensive care unit stay. All subjects are consented and have a HbA1C level drawn to determine if they have diabetes mellitus or not. They are then followed up in 1 year and the HbA1C repeated to determine if they have developed diabetes mellitus over the course.

NCT ID: NCT01970462 Terminated - Clinical trials for Diabetes Mellitus, Type 2

Use of Sitagliptin for Stress Hyperglycemia or Mild Diabetes Following Cardiac Surgery

Start date: January 2014
Phase: Phase 4
Study type: Interventional

This is a randomized controlled trial to determine the safety and efficacy of Sitagliptin in patients with stress hyperglycemia or mild diabetes following cardiac surgery. Patients will receive Sitagliptin or placebo. Sitagliptin may be of particular use in this patient population due to the effects on hepatic glucose production (a major feature of SH), safety (lack of contra-indications for heart failure or renal failure and no hypoglycemia), and tolerability. The secondary objective of this study is to determine whether the management of patients with persistent insulin requirements following cardiac surgery differs among patients with stress hyperglycemia or mild diabetes.

NCT ID: NCT01771133 Terminated - Obesity Clinical Trials

Pregnancy and EARly Lifestyle Improvement Study

PEARLS
Start date: January 2013
Phase: N/A
Study type: Interventional

The investigators propose to conduct a randomized controlled trial in 200 overweight/obese pregnant women and their offspring. The prenatal intervention will emphasize improving diet and physical activity. The lifestyle intervention will be delivered within an empowerment theoretical framework through a combination of group sessions, individual counseling, and by monitoring compliance to diet and physical activity to further tailor the intervention. The post-partum intervention sessions will include mothers and their offspring and will focus on breastfeeding, improving physical activity and quality of the diet and feeding practices through the first post-partum year. As part of routine prenatal care, participants in both the control and intervention arms will be given health-related advice. Since the majority of participants are expected to be eligible for the Women, Infants and Children (WIC) program, both groups will also receive assistance through WIC as per their routine policies. Our primary outcome is Gestational Weight Gain (GWG). The major secondary outcome of interest is infant BMI z-score at 12 months of age, and the investigators will also be evaluating several metabolic outcomes in mothers and infants.

NCT ID: NCT01743313 Terminated - Clinical trials for Hypercholesterolemia

Glucose Metabolism Disorders and Metabolic Syndrome Before and After Primary Hip and Knee Replacement

HyTe-2
Start date: April 2012
Phase:
Study type: Observational

Osteoarthritis patients undergoing primary hip and knee replacement are followed-up and changes in their glucose metabolism and other metabolic parameters (obesity, cholesterol levels) are examined. Persistent postoperative pain is examined as secondary outcome.

NCT ID: NCT01666665 Terminated - Insulin Resistance Clinical Trials

Mechanisms of Improved Wound Healing and Protein Synthesis of Insulin and Metformin

Start date: November 2012
Phase: Phase 2/Phase 3
Study type: Interventional

Massive pediatric burns are associated with a persistent and sustained hypermetabolic response characterized by elevated levels of circulating catecholamine's, cortisol, and glucagon's, which can cause extreme muscle wasting, immunodeficiency, and delay in wound healing. Insulin and metformin have demonstrated anabolic activity with minimal associated side effects. However, it is unknown whether the beneficial effects arise from tight euglycemic control or direct effect of insulin action. We hypothesize that during acute hospitalization, administration of metformin at a dose titrated to maintain blood glucose between 80-180 mg/dl will accelerate wound healing and recovery in children with severe thermal injury and will have beneficial long-term effects on muscle strength, immune function, and wound healing.

NCT ID: NCT01648218 Terminated - Clinical trials for Post-Transplant Glucocorticoid Induced Diabetes

Insulin Therapy for Post-transplant Glucocorticoid Induced Hyperglycemia

PTHG
Start date: August 2012
Phase: Phase 4
Study type: Interventional

No consensus guidelines exist for management of post-transplant glucocorticoid induced hyperglycemia, but most published reviews recommend insulin as first line therapy. A variety of insulin regimens have been proposed, including mealtime short-acting regular or analog insulin, once daily neutral protamine hagedorn (NPH) insulin, pre-mixed insulin, or basal insulin alone such as glargine or detemir. However, no randomized trial has ever examined different insulin regimens to determine which most effectively controls post-transplant steroid-induced hyperglycemia. Consequently, the proposed study intends to examine three commonly used insulin regimens used for managing post-transplant once-daily glucocorticoid-induced hyperglycemia to determine which is most effective: - Group 1: Intermediate-acting (NPH) insulin at breakfast - Group 2: Short-acting insulin (regular or aspart) before meals - Group 3: Insulin glargine at breakfast Question/Hypothesis: Among three commonly used insulin regimens, which is most effective for managing post-transplant once-daily glucocorticoid-induced hyperglycemia?

NCT ID: NCT01486043 Terminated - Diabetes Mellitus Clinical Trials

Metformin and Transient Hyperglycemia

Start date: December 2011
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether metformin is an effective adjunctive treatment for transient hyperglycemia in patients with acute lymphoblastic leukemia (ALL) undergoing induction chemotherapy

NCT ID: NCT01183442 Terminated - Clinical trials for Coronary Artery Disease

Vitamin D Supplementation in CAD and Postchallenge Hyperglycemia

Start date: June 2010
Phase: Phase 3
Study type: Interventional

The main aim of the investigation is to clarify, whether vitamin D supplementation in coronary artery disease patients with vitamin D deficiency and postchallenge hyperglycemia has an impact on endothelial dysfunction and parameters of insulin sensitivity and beta-cell function.