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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02920801
Other study ID # 13040490434
Secondary ID
Status Completed
Phase Phase 4
First received September 29, 2016
Last updated September 30, 2016
Start date December 2014
Est. completion date July 2015

Study information

Verified date September 2016
Source Shanghai Zhongshan Hospital
Contact n/a
Is FDA regulated No
Health authority China: Chinese Medical Association
Study type Interventional

Clinical Trial Summary

In this study, the investigators aim to investigate whether saxagliptin modulate endothelial progenitor cells number and flow-mediated dilation in newly diagnosed, treatment-naive type 2 diabetic patients.


Recruitment information / eligibility

Status Completed
Enrollment 31
Est. completion date July 2015
Est. primary completion date July 2015
Accepts healthy volunteers No
Gender Both
Age group 30 Years to 75 Years
Eligibility Inclusion Criteria:

- newly diagnosed type 2 diabetics (diagnosis were made according to the American Diabetes Association Guideline [19] ), treatment naive, age 30-75, hemoglobin A1c (HbA1c) =6.5%, fasting c-peptide >1.0ng/L

Exclusion Criteria:

- pregnancy or lactation, smoker, acute disease or infection, chronic renal disease (estimated glomerular filtration rate <60 mL/min/1.73m2), live enzymes 3 times above the normal range, positive islet autoantibody, fasting c-peptide <1.0ng/L, severe hypertriglyceridemia (triglyceride >5.6mmol/L), cardiovascular events or surgery within 3 months, taking glucocorticoid, history of acute or chronic pancreatitis, pancreatic tumor, severe cardiac or pneumonic disease.

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Intervention

Drug:
saxagliptin
5mg per day for 12 weeks
Metformin
1500mg per day for 12 weeks

Locations

Country Name City State
China Fang Li Shanghai Shanghai

Sponsors (2)

Lead Sponsor Collaborator
Shanghai Zhongshan Hospital Chinese Medical Association

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary endothelial progenitor cell 12weeks No
Primary flow-mediated dilation 12weeks No
Secondary HbA1c 12weeks No
Secondary fasting blood glucose 12weeks No
Secondary 2 hour postprandial blood glucose 12weeks No
Secondary liver function test 12weeks Yes
Secondary renal function test 12weeks Yes
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