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.
dc.contributor.author | Davis, Stephen N | |
dc.contributor.author | Horton, Edward S | |
dc.contributor.author | Battelino, Tadej | |
dc.contributor.author | Rubin, Richard R | |
dc.contributor.author | Schulman, Kevin A | |
dc.contributor.author | Tamborlane, William V | |
dc.coverage.spatial | United States | |
dc.date.accessioned | 2011-04-15T16:46:24Z | |
dc.date.issued | 2010-04 | |
dc.description.abstract | 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. | |
dc.description.version | Version of Record | |
dc.identifier | ||
dc.identifier.eissn | 1557-8593 | |
dc.identifier.uri | ||
dc.language | eng | |
dc.language.iso | en_US | |
dc.publisher | Mary Ann Liebert Inc | |
dc.relation.ispartof | Diabetes Technol Ther | |
dc.relation.isversionof | 10.1089/dia.2009.0145 | |
dc.relation.journal | Diabetes Technology & Therapeutics | |
dc.subject | Adolescent | |
dc.subject | Adult | |
dc.subject | Aged | |
dc.subject | Child | |
dc.subject | Diabetes Mellitus, Type 1 | |
dc.subject | Humans | |
dc.subject | Hypoglycemic Agents | |
dc.subject | Injections | |
dc.subject | Insulin | |
dc.subject | Insulin Infusion Systems | |
dc.subject | Middle Aged | |
dc.subject | Research Design | |
dc.subject | Young Adult | |
dc.title | 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. | |
dc.type | Journal article | |
duke.date.pubdate | 2010-4-0 | |
duke.description.issue | 4 | |
duke.description.volume | 12 | |
pubs.author-url | ||
pubs.begin-page | 249 | |
pubs.end-page | 255 | |
pubs.issue | 4 | |
pubs.organisational-group | Clinical Science Departments | |
pubs.organisational-group | Duke | |
pubs.organisational-group | Duke Cancer Institute | |
pubs.organisational-group | Duke Clinical Research Institute | |
pubs.organisational-group | Duke Science & Society | |
pubs.organisational-group | Global Health Institute | |
pubs.organisational-group | Initiatives | |
pubs.organisational-group | Institutes and Centers | |
pubs.organisational-group | Institutes and Provost's Academic Units | |
pubs.organisational-group | Medicine | |
pubs.organisational-group | Medicine, General Internal Medicine | |
pubs.organisational-group | School of Medicine | |
pubs.organisational-group | University Institutes and Centers | |
pubs.publication-status | Published | |
pubs.volume | 12 |