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Clinical Trial Summary

This study will evaluate whether the addition of sitagliptin treatment provides additional decrease in HbA1C levels and increase in goal attainment in patients with inadequate glycemic control on their current oral anti-glycemic therapy in real world practice.


Clinical Trial Description

To explore the change of glycemic control (HbA1c or FPG) before and after 24 weeks of Sitagliptin treatment in Type 2 Diabetic patients who have started Sitagliptin as add on therapy during the index period and received Sitagliptin continuously* for at least 24 weeks. ;


Study Design

Time Perspective: Retrospective


Related Conditions & MeSH terms


NCT number NCT01316835
Study type Observational
Source Chang Gung Memorial Hospital
Contact Ching-Jung Hsieh, MD
Phone 886-7-7317123
Email rose@adm.cgmh.org.tw
Status Recruiting
Phase N/A
Start date December 2010
Completion date December 2011

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