STAR 3 randomized controlled trial to compare sensor-augmented insulin pump therapy with multiple daily injections in the treatment of type 1 diabetes: research design, methods, and baseline characteristics of enrolled subjects.
Data(s) |
01/04/2010
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Formato |
249 - 255 |
Identificador |
http://www.ncbi.nlm.nih.gov/pubmed/20210562 Diabetes Technol Ther, 2010, 12 (4), pp. 249 - 255 http://hdl.handle.net/10161/3233 1557-8593 |
Idioma(s) |
ENG en_US |
Relação |
Diabetes Technol Ther 10.1089/dia.2009.0145 Diabetes Technology & Therapeutics |
Tipo |
Journal Article |
Cobertura |
United States |
Resumo |
BACKGROUND: Sensor-augmented pump therapy (SAPT) integrates real-time continuous glucose monitoring (RT-CGM) with continuous subcutaneous insulin infusion (CSII) and offers an alternative to multiple daily injections (MDI). Previous studies provide evidence that SAPT may improve clinical outcomes among people with type 1 diabetes. Sensor-Augmented Pump Therapy for A1c Reduction (STAR) 3 is a multicenter randomized controlled trial comparing the efficacy of SAPT to that of MDI in subjects with type 1 diabetes. METHODS: Subjects were randomized to either continue with MDI or transition to SAPT for 1 year. Subjects in the MDI cohort were allowed to transition to SAPT for 6 months after completion of the study. SAPT subjects who completed the study were also allowed to continue for 6 months. The primary end point was the difference between treatment groups in change in hemoglobin A1c (HbA1c) percentage from baseline to 1 year of treatment. Secondary end points included percentage of subjects with HbA1c < or =7% and without severe hypoglycemia, as well as area under the curve of time spent in normal glycemic ranges. Tertiary end points include percentage of subjects with HbA1c < or =7%, key safety end points, user satisfaction, and responses on standardized assessments. RESULTS: A total of 495 subjects were enrolled, and the baseline characteristics similar between the SAPT and MDI groups. Study completion is anticipated in June 2010. CONCLUSIONS: Results of this randomized controlled trial should help establish whether an integrated RT-CGM and CSII system benefits patients with type 1 diabetes more than MDI. |
Palavras-Chave | #Adolescent #Adult #Aged #Child #Diabetes Mellitus, Type 1 #Humans #Hypoglycemic Agents #Injections #Insulin #Insulin Infusion Systems #Middle Aged #Research Design #Young Adult |