drugset / Trial / NCT01089569
Continuous Glucose Monitoring Evaluation of Exenatide Twice Daily Versus Insulin Glargine
Completed
60 enrolled
HealthPartners Institute
International Diabetes Center at Park Nicollet · collabSanofi · collab
RandomizedParallel-groupOpen-labelTreatment
Summary
The primary purpose of this study is to compare the effect on 24-hour blood glucose patterns, HbA1c, and weight management when adding insulin glargine, or exenatide, or a combination of insulin glargine and exenatide to metformin.
Timeline
- Start
- 2010-04
- Primary completion
- 2013-05
- Completion
- 2013-05
Publications
- Background Mazze RS, Strock E, Wesley D, Borgman S, Morgan B, Bergenstal R, Cuddihy R. Characterizing glucose exposure for individuals with normal glucose tolerance using continuous glucose monitoring and ambulatory glucose profile analysis. Diabetes Technol Ther. 2008 Jun;10(3):149-59. doi: 10.1089/dia.2007.0293.
- Background Mazze R, Strock E, Morgan B, Wesley D, Bergenstal R, Cuddihy R. Diurnal glucose patterns of exenatide once weekly: a 1-year study using continuous glucose monitoring with ambulatory glucose profile analysis. Endocr Pract. 2009 May-Jun;15(4):326-34. doi: 10.4158/EP09046.ORR.
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Comparator | Exenatide | Peptide | 10 ug | — |
| Comparator | insulin glargine | Protein / enzyme biologic | 0.1 iu/kg | — |