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Clinical Trials/JPRN-UMIN000007487
JPRN-UMIN000007487
Recruiting
Phase 4

Blood-Glucose reduction in Type 2 Diabetes Patients when using two different DPP-4, alogliptin or sitagliptin during 52-week administration - Blood-Glucose reduction using DPP-4 agents

Biomedis International Ltd Study Management0 sites300 target enrollmentMarch 20, 2012
ConditionsType 2 diabetes

Overview

Phase
Phase 4
Intervention
Not specified
Conditions
Type 2 diabetes
Sponsor
Biomedis International Ltd Study Management
Enrollment
300
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
March 20, 2012
End Date
September 1, 2014
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Biomedis International Ltd Study Management

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • 1\. Type 1 diabetes or secondary diabetes 2\. Patients with severe infecious disease, operation planned or just after done, and/or serious externalinjyury 3\. Other DPP\-4 agents users on the enrollement 4\. Insulin users 5\. Pregnant and possible pregnant, or Lactation 6\. AST or ALT 2\.5 times or more of normalvalue 7\. Serum creatinine2 mg/dL or more 8\. Patients with old myocardial infarction, angina pectoris and/or stroke 9\. Patients having history of hypersensitivity against study drugs 10\.Inappropriate reasons on the enrollment that the physicians/investigators are judged

Outcomes

Primary Outcomes

Not specified

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