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IDDM clinical trials

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NCT ID: NCT04591925 Terminated - Type 1 Diabetes Clinical Trials

SteadiSetâ„¢ Pilot Study (SteP Study)

Start date: February 5, 2021
Phase: N/A
Study type: Interventional

This study will evaluate the safety and effectiveness of how well blood glucose is managed when a participate wears the investigational SteadiSetâ„¢ Infusion Set (SteadiSet device) for up to 14 days post-insertion when compared to a Teflon Control infusion set.

NCT ID: NCT01781975 Completed - Clinical trials for Type 1 Diabetes Mellitus

Imatinib Treatment in Recent Onset Type 1 Diabetes Mellitus

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

Type 1 diabetes mellitus (T1DM) results from the autoimmune destruction of insulin-producing ß cells. Although exogenous insulin is widely available, it is not possible for affected individuals to consistently achieve euglycemia with current technology, and thus they are at risk for devastating long-term complications. This phase II study is designed to evaluate the safety and efficacy of imatinib mesylate as a novel therapy for new-onset T1DM. Imatinib is a first-in-class tyrosine kinase inhibitor. This study will explore the potential role of short-term therapy with imatinib to induce tolerance and possibly lead to a durable long-term remission of T1DM.

NCT ID: NCT00502138 Completed - IDDM Clinical Trials

A Pilot Study of Continuous Subcutaneous Pramlintide Infusion Therapy in Patients With Type 1 Diabetes

Start date: July 2007
Phase: Phase 4
Study type: Interventional

This research project will investigate the effects of pramlintide (Symlin) given by continuous subcutaneous (under the skin) infusion throughout the day and night, along with meal doses similar to those injected during conventional pramlintide (Symlin) treatment, delivered using a second insulin pump, in subjects with inadequately controlled type I diabetes mellitus who are already using insulin pump therapy. Study participants will wear two pumps for a four month period, taking insulin in their usual manner and pramlintide (Symlin) in a similar basal/bolus fashion. Continuous glucose monitors will be worn on three occasions during the study to assess blood glucose responses to continuous pramlintide (Symlin) treatment.