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Type 2 Diabetes clinical trials

View clinical trials related to Type 2 Diabetes.

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NCT ID: NCT00442884 Completed - Type 2 Diabetes Clinical Trials

Effect of Acute Psychological Stress on Glucose Concentrations in Patients With Type 2 Diabetes

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

The study is designed to evaluate the effects of acute psychological stress on blood glucose levels. We will study one group of patients in the fasting state on a control day and a stress test day, another group will undergo the same protocol in the postprandial state.

NCT ID: NCT00441363 Terminated - Type 2 Diabetes Clinical Trials

Efficacy and Safety of Cycloset® Compared With Placebo When Added to Metformin

Start date: February 2005
Phase: Phase 3
Study type: Interventional

The purpose of this study is to investigate the efficacy and safety of Cycloset® and placebo when added to metformin monotherapy (at least 1000 mg/day for 3 months prior to screening) in persons with type 2 diabetes mellitus who are not adequately controlled on metformin therapy alone.

NCT ID: NCT00440284 Active, not recruiting - Type 2 Diabetes Clinical Trials

Flexible, Intensive vs. Conventional Insulin Therapy in Insulin-Naive Adults With Type 2 Diabetes

Start date: January 2004
Phase: Phase 3
Study type: Interventional

Objective. Flexible, intensive insulin therapy (FIT) with pre-prandial regular insulin and conventional insulin therapy (CIT) with twice daily premixed insulin are treatment options in patients with type 2 diabetes who become insulin dependent. While intensive insulin therapy can increase meal and life style flexibility, conventional therapy is easier to perform. The aim of the study was to compare metabolic outcomes and patient preferences of both treatment regimens. Research Design and Methods. Non-blinded, randomized controlled cross-over clinical pilot trial. Insulin naive participants who failed therapeutic goals under oral antidiabetic therapy underwent FIT and CIT for two months. Patients completed standard Diabetes Treatment and Teaching Programs (DTTP) and trained FIT and CIT. Main outcome measures were glycosylated hemoglobin (GHb), mild and severe hypoglycemia, insulin dosage, blood pressure and body-mass-index (BMI). Before/after and inter-group analyses were performed. Finally, therapy preference was analyzed.

NCT ID: NCT00438698 Completed - Type 2 Diabetes Clinical Trials

Low Glycemic Index Diets vs. High Cereal Fibre Diets in Type 2 Diabetes

Start date: September 2004
Phase: N/A
Study type: Interventional

Large observational studies have shown cereal fiber to protect from diabetes and heart disease. Despite the success of acarbose, an α-glucosidase hydrolase inhibitor, which lowers the glycemic index of foods containing starch, sucrose and maltodextrins, the use of diets containing low glycemic index foods still remains to be established. We will therefore provide otherwise healthy individuals with type 2 diabetes intensive counseling on food selection either to improve glucose control using high cereal fiber dietary strategies or low glycemic index foods. Studies will last 6 months with bloods taken for HbA1c, glucose and blood lipids. If the study shows a benefit for either or both diets then use of high fiber and/or low glycemic index foods in the diet may provide another potential way to improve glucose control and lower cholesterol levels in non-insulin dependent diabetes.

NCT ID: NCT00434499 Withdrawn - Obesity Clinical Trials

Effect of EGCG on the Body's Response to Insulin

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

This study will examine whether epigallocatechin gallate (EGCG), a major component of green tea, affects how the body responds to insulin in healthy and obese people. Insulin is not as effective in people who are overweight, have high blood pressure or diabetes. This condition is known as insulin resistance. Laboratory studies suggest that green tea or EGCG treatment lowers blood pressure, lowers blood sugar and increases blood flow. This study will see if EGCG improves insulin resistance or insulin's effects on blood flow in people with insulin resistance. Healthy normal weight or overweight people between 21 and 65 years of age may be eligible for this study. Participants are randomly assigned to take EGCG or a placebo ( inactive dummy pill ) in two 4-week treatment phases with a 2-week period of no study medication before each treatment phase. After the first 4-week treatment, patients on placebo are switched to EGCG and those on EGCG are switched to placebo. In addition to treatment, participants undergo the following procedures during the study period: - Screening, including medical history, physical examination and blood and urine tests, and finger-stick blood sugar measurement for patients with diabetes - Complete a dietary and physical activity questionnaire and consult with a dietitian - Blood and urine tests - At-home and clinic blood pressure monitoring - Glucose clamp test to measure how the body responds to insulin. This test is done three times during the study. A needle is placed in a vein in each of the subject's arms, one for sampling blood and the other for infusing insulin, glucose and potassium. Glucose and insulin levels, electrolytes, lipids, fatty acids, cytokines and epicatechin are measured. - Forearm blood flow measurement with microbubbles and ultrasound. Before beginning the glucose clamp test, a test of how well the blood vessels relax is done. A device that measures the size of the artery in the upper arm is placed above the elbow. Blood flow in the muscle of the forearm is measured by ultrasound using a small infusion through a vein of microbubble contrast agent consisting of gas-filled bubbles the size of red blood cells. The contrast agent is infused over a 7- to 9-minute period at the beginning of the glucose clamp test and again 2 hours after the beginning of the test.

NCT ID: NCT00428571 Terminated - Type 2 Diabetes Clinical Trials

Laparoscopic Bariatric Surgery to Treat Type 2 Diabetes in Obese Patients

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

A large number of research studies on people who were morbidly obese (extremely overweight), and had bariatric surgery (anti-obesity surgery) have shown that patients who were diabetic before surgery often experienced significant improvement in their diabetes following the surgery. For some patients, blood glucose levels returned to the normal range, and they were able to stop taking all of their diabetes medications. For others, blood glucose levels improved, allowing them to reduce their diabetes medications. This research study is being done to determine whether bariatric surgery can safely provide better control of diabetes symptoms in obese diabetics than continuing medical management (anti-diabetic drugs in combination with diet and lifestyle changes). There are several different types of bariatric surgery currently being used to treat morbid obesity. Two of the most common techniques are gastric bypass and adjustable gastric banding. This study will be comparing these two surgical techniques to treatment with a combination of drugs, diet, and lifestyle changes for control of type 2 diabetes.

NCT ID: NCT00425269 Completed - Type 2 Diabetes Clinical Trials

Lifestyle Intervention for Pakistani Women in Oslo

InnvaDiab
Start date: April 2006
Phase: N/A
Study type: Interventional

Immigrants from South Asia in Norway have a high prevalence of type 2 diabetes and conditions related to the metabolic syndrome. It has been documented that these conditions may be prevented by changes in lifestyle. No previous intervention studies on immigrants with focus on diet and physical activity have been carried out in Norway. This project concerns a randomized controlled trial with intervention to change diet and physical activity in 200 high risk female Pakistani immigrants living in Oslo. The intervention will be evaluated both in terms of outcome and process.

NCT ID: NCT00425009 Completed - Type 2 Diabetes Clinical Trials

Therapeutic Effects of Berberine in Patients With Type 2 Diabetes

Start date: January 2004
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to determine whether berberine is effective in the treatment of type 2 diabetes.

NCT ID: NCT00422253 Completed - Obesity Clinical Trials

Dietary Advanced Glycation End-products and Insulin Resistance in Overweight and Obese Humans

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

We hypothesize that reduction in dietary advance glycation endproducts (AGE) intake will increase insulin sensitivity and normalise insulin secretion in overweight and obese individuals through reduction of chronic low grade inflammation. We propose to test this hypothesis by performing euglycemic hypeinsulinemic glucose clamp and intravenous glucose tolerance test before and after low AGE diet and normal Australian diet in a cross-over design. This study will provide information relevant to the development and prevention of type 2 diabetes.

NCT ID: NCT00419484 Completed - Hypertension Clinical Trials

Effect of Pioglitazone on Cardiovascular Outcome on Higashi-Saitama Trial in Patients With Type 2 Diabetes

Start date: March 2004
Phase: Phase 4
Study type: Observational

We want to investigate the effects of pioglitazone on cardiovascular events in Japanese patients with type 2 diabetes.