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Type 1 Diabetes clinical trials

View clinical trials related to Type 1 Diabetes.

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NCT ID: NCT01536431 Completed - Type 1 Diabetes Clinical Trials

Safety Study to Assess Whether Proinsulin Peptide Injections Can Slow or Stop the Body Damaging Its Own Insulin-making Cells in the Pancreas in Patients Newly Diagnosed With Type 1 Diabetes

MonoPepT1De
Start date: January 2012
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to address the safety issue of whether, in patients with newly−diagnosed diabetes who still make some insulin, proinsulin peptide therapy adversely affects the rate of damage to the insulin making cells.

NCT ID: NCT01531855 Completed - Type 1 Diabetes Clinical Trials

Post-exercise Insulin Reductions in Type 1 Diabetes

Start date: February 2012
Phase: N/A
Study type: Interventional

The investigators hypothesise that reducing rapid-acting insulin dose after exercise will help prevent Type 1 diabetes individuals experiencing hypoglycaemia.

NCT ID: NCT01530347 Terminated - Type 1 Diabetes Clinical Trials

Non Invasive Breath Based Acetone-meter- Easy Check

Start date: March 2012
Phase: Phase 1
Study type: Interventional

Segment 1- this segment will include two main steps: Step 1-Calibration: During this step we plan to collect paired measurements of capillary blood glucose using reference method and data generated by the non invasive study device. Samples will be obtained at specific time points during 4 hours: at fasting, and after consuming standard liquid meal at 60, 120, 180 and 240 minutes. At each time point capillary blood glucose will be measured using the invasive reference method. The paired reference and study device data will be analyzed using multivariate regression model to formulate a calibration algorithm model. This model will convert the acetone values measured by study device to blood glucose values. step 2-Validation: During this segment the second step of this segment we plan to evaluate the validity and reliability of the non-invasive breath-based glucometer compared to standard invasive reference glucometer. Results will be compared using a Clark error grid. Segment 2- During this segment we plan to collect paired measurements of capillary blood glucose beta Hydroxybutyrate using reference method and acetone values generated by the non invasive breath based study device. Samples will be obtained at specific time points during 4 hours after overnight fasting, while basal insulin will be suspended, which is accepted to produce ketosis.

NCT ID: NCT01527981 Completed - Depression Clinical Trials

Cognitive Behavioral Therapy (CBT) for Adherence and Depression in Type 1 Diabetes

Start date: March 2008
Phase: Phase 2
Study type: Interventional

This study is a pilot behavioral intervention trial, designed to initially examine cognitive behavioral therapy for medical adherence and depression (CBT-AD) in patients with depression and poorly controlled type 1 diabetes.

NCT ID: NCT01521520 Active, not recruiting - Type 1 Diabetes Clinical Trials

Imaging of Type 1 Diabetes Progression

Start date: January 2012
Phase: N/A
Study type: Observational

Type 1 diabetes results from the autoimmune destruction of the insulin-producing beta cells of the islets of Langerhans of the pancreas. Initially, diabetes is usually clinically silent with immune cells invading the pancreatic islets, a process termed insulitis, which eventually leads to loss of beta cells in the islets. If enough beta cells are destroyed, the body can not make enough insulin to maintain blood sugars in the normal range and clinical diabetes develops. The purpose of this study is to assess the ability of magnetic resonance imaging with ferumoxytol to detect changes in the pancreas associated with the insulitis of type 1 diabetes.

NCT ID: NCT01519466 Completed - Type 1 Diabetes Clinical Trials

Impact of a built-in Insulin Calculator Feature on Diabetes Control - Pilot Study

Start date: January 2012
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate the effect of using FreeStyle InsuLinx (a blood glucose meter with a built-in insulin calculator) on glucose control in people with type 1 diabetes.

NCT ID: NCT01519102 Completed - Type-1 Diabetes Clinical Trials

Comparison of Closed-loop Operation After Morning Meal With and Without Carbohydrate Counting

CLASS02
Start date: January 2012
Phase: Phase 2
Study type: Interventional

Closed-loop strategy is composed of three components: glucose sensor to read glucose levels, insulin pump to infuse insulin and a dosing mathematical algorithm to decide on the required insulin dosage based on the sensor's readings. A dual-hormone closed-loop system would regulate glucose levels through the infusion of two hormones: insulin and glucagon. The main goal of this project is to assess whether a dual-hormone closed-loop strategy would alleviate the burden of carbohydrate counting from patients with type 1 diabetes (T1D) without a significant degradation in post-meal glucose control. Each patient will be admitted twice to a clinical research facility. In one visit, patients will eat a morning meal accompanied with a matching insulin bolus (depending on the carbohydrate content of the meal) and glucose levels will be subsequently regulated using dual-hormone closed-loop system. In the other visit, patients will eat the same meal but will inject only a partial insulin bolus (not depending on carbohydrate content of the meal) and the remaining needed insulin will be delivered based on glucose sensor excursions as part of closed-loop operation. If post-meal glucose levels were indifferent between the two visits, then this would suggest that carbohydrate counting may not be necessary during closed-loop operation as the closed-loop system will give any remaining insulin needed to cover the glucose absorbed from the meal. Twelve subjects will be enrolled in this study.

NCT ID: NCT01517269 Completed - Type 1 Diabetes Clinical Trials

PETS-D (Parent Education Thru Simulation-Diabetes)

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

Hypothesis: Parents who receive Parent Education Thru Simulation-Diabetes (PETS-D) will have significantly higher diabetes knowledge (cognitive visual schemata), better technical and problem-solving competence and confidence, and lower fear and stress/anxiety levels; and provide better diabetes management at 14 weeks compared to those parents receiving standard diabetes education.

NCT ID: NCT01515384 Terminated - Type 2 Diabetes Clinical Trials

A Trial of 18F-AV-133 Positron Emission Tomography (PET)

Start date: June 2010
Phase: Phase 1
Study type: Interventional

The purpose of this study is to evaluate the safety and pancreas imaging properties of 18F-AV-133.

NCT ID: NCT01513746 Completed - Type 1 Diabetes Clinical Trials

Eating Disorders in Type 1 Diabetes: Mechanisms of Comorbidity

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

The purpose of the study is to investigate how people with type 1 diabetes experience and manage their diabetes, eating, and weight. Summary of the Study: If you choose to participate, you will complete a set of questionnaires and a structured interview. You will then wear a continuous glucose monitor and use your cell phone to answer study questions for a period of 3 days. The questions come in the form of regular phone calls between the hours of 8:00 a.m. and 10:00 p.m. Each call takes only a minute or two to complete. You will also be asked to call in and answer study questions at other times during the day, especially after eating. The study involves a minimum of 2 clinic visits to Duke. Participants who live greater than 1.5 hours from Duke can be approved to take part in the study by phone/Skype. Participants will receive and return study materials through the mail.