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Clinical Trials/JPRN-UMIN000015478
JPRN-UMIN000015478
Completed
未知

A study on the efficacy and biogenic adaptability affected by ipragliflozin - A study on the efficacy and biogenic adaptability affected by ipragliflozin

Kobe University0 sites104 target enrollmentJuly 1, 2015
ConditionsType 2 diabetes

Overview

Phase
未知
Intervention
Not specified
Conditions
Type 2 diabetes
Sponsor
Kobe University
Enrollment
104
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

After SGLT2 inhibitor adoministration, appetite of participants increased, and the level of plasma leptin levels increased.

Registry
who.int
Start Date
July 1, 2015
End Date
November 16, 2017
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • 1\) Type 1 diabetes 2\) With severe ketosis, diabetic coma, or precoma within 6 months 3\) With severe infection, pre or post surgery, and serious trauma 4\) With severe hepatic dysfunction 5\) With renal dysfunction (Serum Creatinine male: \>\= 1\.5 mg/dL, female: \>\= 1\.3 mg/dL) 6\) Is receiving steroids 7\) Has history of gastrectomy (include segmentectomy and total resection, but not endoscopic mucosal resection) 8\) Has stroke, myocardial infarction, or other serious cardiovascular complications requiring hospitalization within 6 months at consent 9\) Has history of receiving SGLT\-2 inhibitor 10\) Is pregnant, nursing, or planned to become pregnant 11\) Has history of hypersensitivity to ipragliflozin or any other excipient of ipragliflozin 12\) Considered as inadequate by the investigator

Outcomes

Primary Outcomes

Not specified

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