A Phase 4 interventional study of Insulin LISPRO in Diabetes Mellitus, Type 2, sponsored by Sun Yat-sen University. Completed at 1 site in China. Open to participants aged 20 Years to 75 Years. Per ClinicalTrials.gov, last updated 2018-04-26.
Sponsored by Sun Yat-sen University · Phase 4, Interventional, and Treatment
The purpose of this study is to investigate and evaluate the significance of intravenous glucose tolerance test in assessment of β-cell function improvement after short course of intensive insulin therapy, trying to illustrate the relationship between fasting plasma glucose and acute insulin release under different stage of type 2 diabetes with poor glycemic control.
10,925 studies on the registry are indexed under Diabetes Mellitus; 1,318 are open to participants now.
This study's enrollment of 67 is below the median of 80 across 8,367 interventional studies indexed under Diabetes Mellitus.
Browse Diabetes Mellitus studies →Sun Yat-sen University is the lead sponsor of 1,644 studies on the registry; 602 are open to participants now.
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Inclusion Criteria: different course of type 2 diabetes with poor glycemic control
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Exclusion Criteria:
different duration of disease receive insulin LISPRO
Drug: Insulin LISPRO
receive short-term insulin pump therapy by using insulin LISPRO, continue treatment for 7 more days when euglycemia achieved
Also known as: humalog
fasting plasma glucose after insulin therapy
Time frame: 10 hour
This study is completed, as verified in Apr 2018. You cannot join it, but the record below documents what was studied.
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Sun Yat-sen University