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Hyperglycemia clinical trials

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NCT ID: NCT00666250 Completed - Hypertension Clinical Trials

Effects of Xoçai Antioxidant Supplements on Atherosclerosis Risk Factors

Start date: January 2006
Phase: N/A
Study type: Interventional

An antioxidant dietary supplement made from cocoa powder, and extracts of acai, grape and blueberry will be tested for effects on blood sugar, blood pressure, cholesterol and related parameters in human subjects.

NCT ID: NCT00666094 Completed - Clinical trials for Diabetes Mellitus, Type 2

A Randomized Controlled Trial of Exercise Training Among Men With Type 2-diabetes

Start date: August 2008
Phase: N/A
Study type: Interventional

To test the hypothesis that there is no difference in change in HbA1C among men with type 2-diabetes after an exercise intervention with strength versus endurance training.

NCT ID: NCT00663624 Withdrawn - Diabetes Clinical Trials

Management of Hyperglycemia in the ER: A Randomized Clinical Trial of a Subcutaneous Insulin Aspart Protocol Coupled With Rapid Initiation of Basal Bolus Insulin Prior to Hospital Admission Versus Usual Care

NOVO ER
Start date: n/a
Phase: Phase 4
Study type: Interventional

In the Emergency Department (ED), diabetes is commonly encountered as a secondary diagnosis and many patients with uncontrolled diabetes are admitted to the hospital after initial evaluation in the ED. Currently there are no guidelines in the US for the management of hyperglycemia in patients with diabetes during the duration of evaluation and treatment in the ED. It is known that high blood glucose levels in hospitalized patients with diabetes are associated with increased risk of medical complications. In this study, we hypothesize that a defined two-step approach to the management of high blood sugars with insulin injections initiated in the ED may decrease length of stay in the ED or hospital, improve clinical outcome and prevent some hospital complications. In the first phase, patients with diabetes admitted to the ED that have a high blood sugar (BG 200mg/dL) will be randomized to receive scheduled aspart or the usual care as dictated by the ED physicians. In the second phase, patients enrolled in the first phase that are subsequently admitted to the hospital will receive a combination of detemir and aspart insulin or usual care as dictated by the Admitting Medicine Team. Detemir is a long-acting insulin which is given subcutaneously (under the skin) once daily. Aspart is a rapid-acting insulin which is given subcutaneously several times a day and frequently before meals. Detemir and aspart insulins are approved for use in the treatment of patients with diabetes by the FDA. Usual care can be oral anti-diabetic agents, subcutaneous insulin therapy or a combination of both. Subcutaneous insulin used for usual care could include NPH, 70/30 insulin, aspart insulin, regular insulin or insulin glargine. This investigator-initiated research will be conducted at Grady Memorial Hospital, Atlanta and at Rush University Medical Center, Chicago, IL. Dr. Smiley will serve as principal investigator at the Atlanta site. A total of 120 patients will be recruited at Grady and 120 patients at the Rush University Medical Center, Chicago, IL. This study is supported by Novo Nordisk.

NCT ID: NCT00656682 Completed - Obesity Clinical Trials

Primary Care Community Partnerships to Prevent Diabetes

RAPID
Start date: April 2008
Phase: N/A
Study type: Interventional

The purpose of this study is to determine if providing free-of-charge access to a group-based lifestyle intervention delivered in partnership with the community is cost-effective for the prevention of type 2 diabetes.

NCT ID: NCT00655460 Recruiting - Hyperglycemia Clinical Trials

Improving Blood Glucose Control With a Computerized Decision Support Tool: Phase 1

Start date: February 2006
Phase: Phase 2
Study type: Interventional

The Purpose of this study is to: 1. Refine and validate a computerized bedside decision support tool blood glucose management in critically ill adult and pediatric ICU patients. 2. Monitor how often low blood sugar levels occur during use of the bedside tool. 3. Determine how the computerized tool effects the workload of the ICU nurses.

NCT ID: NCT00654797 Recruiting - Hyperglycemia Clinical Trials

Improving Blood Glucose Control With a Computerized Decision Support Tool: Phase 2

Start date: September 2007
Phase: Phase 2
Study type: Interventional

The Purpose of this study is to: 1. Introduce the refined, validated, and safe computerized bedside decision support tool for blood glucose management in critically ill adult and pediatric ICU patients that was studied in Phase 1 into a second group of naïve ICUs, none of which participated in eProtocol-insulin development, refinement or validation 2. Monitor how often low blood sugar levels occur during use of the bedside tool. 3. Determine how the computerized tool effects the workload of the ICU nurses.

NCT ID: NCT00653510 Completed - Clinical trials for Type 2 Diabetes Mellitus

The Metabolic Effects of Acute Hyperglycemia in Patients With Type 2 Diabetes

Start date: March 2008
Phase: N/A
Study type: Interventional

The purpose of the study is to characterize the changes in amino acid, lipid and glucose metabolism in patients with type 2 diabetes exposed to acute hyperglycemia. Moreover we wish to assess the effect of acute hyperglycemia on cardiac output.

NCT ID: NCT00640991 Completed - Clinical trials for Cardiovascular Diseases

REsearching Coronary REduction by Appropriately Targeting Euglycemia (RECREATE Pilot Study)

RECREATE Pilot
Start date: April 2008
Phase: Phase 3
Study type: Interventional

Insulin will safely reduce glucose levels in patients with acute ST-elevation myocardial infarction and admission hyperglycemia.

NCT ID: NCT00636714 Completed - Clinical trials for Hyperglycemia in Critically Ill Patients

Comparison of 2 Methods to Achieve Tight Glucose Control in Cardiovascular ICU Patients

Start date: January 2008
Phase: Phase 4
Study type: Interventional

There is current evidence that maintaining ICU patient's blood sugar between 4.4-6.1 saves lives. However, this is difficult to do in the ICU and carries risks of lowering the blood sugar too much. In addition, the best way to achieve this control is not known. Many strict nomograms that provide a standardized approach for nurses have been developed and validated, including one here at SMH. However, these nomograms cannot apply to all patients at all times, especially ICU patients whose needs are rapidly changing. ICU nurses are at the bedside constantly, are very familiar with their patient's needs, and have decades of experience in titrating medication doses without a nomogram to achieve a pre-determined response (i.e. medications to achieve pre-selected blood pressure). Indeed, once the bedside nurse has bought into the importance of the concept of tight glucose control and have been introduced to the nomogram here at SMH, their experience and intuition may be more adaptable to the changing needs of the patient than an inflexible paper nomogram. This study will compare glucose control using our current standard nomogram versus no nomogram (i.e. nurse directed) in order to determine whether the nomogram should continue to be used.

NCT ID: NCT00626041 Recruiting - Hypertension Clinical Trials

U-CHAMP: Urban Cardiovascular Health Assessment and Management Program

U-CHAMP
Start date: February 2008
Phase: N/A
Study type: Interventional

High blood pressure, elevated blood glucose and high cholesterol are related to the increased risk of stroke and heart disease. Many studies have shown that this risk can be significantly reduced by lowering blood pressure, blood glucose and cholesterol levels. Through a collaborative effort between Calgary Safeway pharmacists and Calgary Health Region family physician PCN's, U-CHAMP will deliver a program to assist in the identification and management of people with elevated blood pressure, blood glucose and cholesterol and through this effort, reduce the risk of heart disease and stroke in the urban Calgary population aged 18-85 years.