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

被引:31
作者
Davis, Stephen N. [1 ]
Horton, Edward S. [2 ]
Battelino, Tadej [3 ]
Rubin, Richard R. [4 ]
Schulman, Kevin A. [5 ]
Tamborlane, William V. [6 ]
机构
[1] Vanderbilt Univ, Dept Med, Nashville, TN 37232 USA
[2] Joslin Diabet Ctr, Boston, MA 02215 USA
[3] Univ Childrens Hosp, Ljubljana, Slovenia
[4] Johns Hopkins Univ, Baltimore, MD USA
[5] Duke Univ, Durham, NC USA
[6] Yale Univ, New Haven, CT USA
关键词
QUALITY-OF-LIFE; INFUSION; CHILDREN; HYPOGLYCEMIA; ADOLESCENTS; MELLITUS; SYSTEM;
D O I
10.1089/dia.2009.0145
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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 <= 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 <= 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.
引用
收藏
页码:249 / 255
页数:7
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