1038-P: Results of Interim Analysis of a Randomized Crossover Study in Type 1 Diabetes (T1D) of a Dual-Hormone Closed-Loop System with Xerisol™ Glucagon vs. Insulin-Only Closed-Loop System vs. a Predictive Low Glucose Suspend System
العنوان: | 1038-P: Results of Interim Analysis of a Randomized Crossover Study in Type 1 Diabetes (T1D) of a Dual-Hormone Closed-Loop System with Xerisol™ Glucagon vs. Insulin-Only Closed-Loop System vs. a Predictive Low Glucose Suspend System |
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المؤلفون: | Peter G. Jacobs, Joseph Leitschuh, Jessica R. Castle, Navid Resalat, Leah M. Wilson, Brian Senf, Joseph El Youssef, Ravi Reddy, Virginia Gabo, Deborah Branigan |
المصدر: | Diabetes. 68 |
بيانات النشر: | American Diabetes Association, 2019. |
سنة النشر: | 2019 |
مصطلحات موضوعية: | 0301 basic medicine, medicine.medical_specialty, Type 1 diabetes, business.industry, Endocrinology, Diabetes and Metabolism, Insulin, medicine.medical_treatment, 030209 endocrinology & metabolism, Hypoglycemia, medicine.disease, Glucagon, Artificial pancreas, Crossover study, 03 medical and health sciences, 030104 developmental biology, 0302 clinical medicine, Internal medicine, Diabetes mellitus, Internal Medicine, medicine, Aerobic exercise, business |
الوصف: | Dual-hormone systems show promise to reduce hypoglycemia, but require a stable liquid glucagon formulation. XeriSol™ glucagon is a shelf-stable glucagon product for this use. Nineteen subjects with T1D are completing a single-center three-day outpatient study comparing control modes of the Oregon Artificial Pancreas system: 1) dual hormone (DH) closed-loop with Novolog™ insulin and XeriSol™ glucagon, 2) insulin-only single hormone (SH) closed-loop, 3) insulin-only predictive low glucose suspend system (PLGS). In clinic aerobic exercise (45 minutes at 60% VO2max) and home exercise was completed with each arm. SH and DH used automated exercise detection to adaptively dose insulin/glucagon for predicted hypoglycemia and tailored mealtime dosing based on past meal responses with an adaptive algorithm. An interim analysis after 7 subjects was completed for safety. The primary outcome measures are % time 70-180 mg/dL and % time Disclosure L.M. Wilson: None. P.G. Jacobs: Stock/Shareholder; Self; Pacific Diabetes Technologies. N. Resalat: None. R. Reddy: None. J. El Youssef: None. D. Branigan: None. J.A. Leitschuh: Other Relationship; Self; AgaMatrix. B. Senf: None. V. Gabo: None. J.R. Castle: Advisory Panel; Self; Novo Nordisk Inc., Zealand Pharma A/S. Consultant; Self; Dexcom, Inc. Research Support; Self; Dexcom, Inc., Xeris Pharmaceuticals, Inc. Funding JDRF |
تدمد: | 1939-327X 0012-1797 |
الوصول الحر: | https://explore.openaire.eu/search/publication?articleId=doi_________::1c261303c3e7c99b04c3f16d7df87e07Test https://doi.org/10.2337/db19-1038-pTest |
حقوق: | CLOSED |
رقم الانضمام: | edsair.doi...........1c261303c3e7c99b04c3f16d7df87e07 |
قاعدة البيانات: | OpenAIRE |
تدمد: | 1939327X 00121797 |
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