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Blood Glucose clinical trials

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NCT ID: NCT00984737 Completed - Diabetes Mellitus Clinical Trials

Hyperglycemia in a Coronary Intensive Care Unit

Start date: May 2007
Phase: N/A
Study type: Interventional

Newly diagnosed hyperglycemia (NDH) and stress hyperglycemia (SH) during acute illness is reported as a non-physiological condition in hospitals. The investigators aim is to determine the rate of NDH and SH among cases admitted to coronary ICU with acute coronary disease and to inquire the relationship of SH with disease severity and functional outcomes such as longevity of ICU stay.

NCT ID: NCT00935922 Completed - Body Weight Clinical Trials

CCRC: Understanding the Effects of Omega-3 Fatty Acids Versus Lignans in Flaxseed on Metabolic and Inflammatory Markers Leading to Diabetes and Cardiovascular Disease

Start date: February 2009
Phase: N/A
Study type: Interventional

The aim of this study is to compare the effects of flaxseed on atherogenic lipids, plasma inflammatory markers, and insulin sensitivity. We hypothesize that flaxseed omega-3 fatty acids will improve the lipid profile (decrease triglyceride, total and LDL-cholesterol and increase HDL-cholesterol). Flaxseed is the richest dietary source of lignan secoisolariciresinol diglucoside (SDG). Lignans are estrogens found in plant sources that behave similar to endogenous estrogens and have been associated with cardiovascular benefits due to their antioxidant activity. Therefore, we also hypothesize that flax-lignans will cause a significant decrease in LDL oxidation and in inflammatory markers such as C-reactive protein (CRP), interleukin-6 (IL-6), IL-1B, serum fatty acid binding protein 4 (FABP-4), and serum amyloid attached to high density lipoprotein (HDL-SAA).

NCT ID: NCT00906490 Completed - Blood Glucose Clinical Trials

Clinical Study of the Intravenous Blood Glucose System in Hospitalized Adult Elective or Non-Emergent Surgery and Medical/Surgical Intensive Care Unit Patients

Start date: June 2009
Phase: N/A
Study type: Observational

The primary objective of this study is to evaluate the performance and safety of the intravenous blood glucose (IVBG) System relative to point of care (POC) meter performance when each method is compared to the Yellow Springs Instrument (YSI) under various conditions in the operating room (OR), ICU and general ward (GW) in subjects undergoing elective or non-emergent surgery as well as subjects admitted to the medical/surgical ICU. POC meter systems are currently used in the hospital environment to measure blood glucose values. The YSI is an accepted reference standard for assessing POC meter accuracy. The secondary objective of this study is to evaluate the performance of the IVBG System as compared with the YSI under various conditions in the operating room (OR), intensive care unit (ICU) and general ward (GW) in subjects undergoing elective or non-emergent surgery as well as subjects admitted to the medical/surgical ICU.

NCT ID: NCT00596128 Completed - Blood Glucose Clinical Trials

Standard Operating Procedures in Daily Clinical Routine

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

Primary study endpoint: blood sugar values Patients: Patients admitted to an ICU 5 steps: 1. Routine treatment, 2. Implementation of SOP for blood sugar monitoring and intervention, 3. Education of intensive care nurses, 4. 6 months free interval without further education or check-up of SOP implementation, 5. Check of SOP implementation and clinical outcome concerning range of blood sugar

NCT ID: NCT00486681 Completed - Diabetes Mellitus Clinical Trials

Clinical Assessment of an in-Patient Glucose Monitoring System (Accu-Chek Inform Cobas IT 1000)

COBAS
Start date: January 2007
Phase: N/A
Study type: Observational

The principal objective of this single-center 2-period study is to evaluate the glycemic control of in-patients in 3 hospital departments (Diabetology, Cardiology and Pulmonary Care) as the rate of capillary blood glucose measurements within a pre-define target range, and to compare results during the period I (warning of the Accu-Check Inform glucose meter on glucose levels not activated) and period II (warning activated).

NCT ID: NCT00444171 Completed - Blood Glucose Clinical Trials

Glucose Control by eMPC Algorithm in Peri- and Postoperative Period in Cardiac Surgery Patients

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

Randomized controlled trial to compare blood glucose control by the model predictive control algorithm with variable sampling rate (eMPC) with routine glucose management protocol (RMP) in peri- and postoperative period in cardiac surgery patients.

NCT ID: NCT00302302 Completed - Blood Glucose Clinical Trials

The Effects of L-arabinose on Intestinal Sucrase Activity in Man

Start date: September 2005
Phase: Phase 1
Study type: Interventional

The purpose of this study is to investigate the effect of L-arabinose in a sugar-rich meal on intestinal sucrase activity in healthy volunteers by measuring postprandial blood glucose and insulin, and selected intestinal hormonal responses to increasing doses of L-arabinose.