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Clinical Trials/JPRN-UMIN000019462
JPRN-UMIN000019462
Completed
未知

Investigation of factors which are related to urinary volume change after canagliflozin administration - Investigation of factors which are related to urinary volume change after canagliflozin administration

Medical Corporation Hokubukai Utsukushigaoka Hospital, Clinical Pharmacology Center0 sites12 target enrollmentOctober 26, 2015

Overview

Phase
未知
Intervention
Not specified
Conditions
Type2 diabetes mellitus
Sponsor
Medical Corporation Hokubukai Utsukushigaoka Hospital, Clinical Pharmacology Center
Enrollment
12
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
October 26, 2015
End Date
December 15, 2015
Last Updated
2 years ago
Study Type
Interventional
Sex
All

Investigators

Sponsor
Medical Corporation Hokubukai Utsukushigaoka Hospital, Clinical Pharmacology Center

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • 1\. Patients who have not received treatment of type 2 diabetes mellitus(diet therapy, exercise therapy, oral hypoglycemic agent and so on) 2\. Patient with type 1 diabetes mellitus or with history of secondary diabetes mellitus 3\. Patients who have experienced repeated severe hypoglycemic episodes 4\. Patients with the history of serious diabetic complications requiring treatment 5\. Patients treated with insulin, GLP\-1 receptor agonist, SGLT\-2 inhibitor, diuretic (including drug combination) 6\. Patients with history of , or concurrent complication that affect renal function(renal disease, renal stone, prostatic inflammation and so on) , or patients with urinary\-tract infection 7\. Patients with history of drug or food allergies 8\. Patients with history of myocardial infarction, congestive heart failure, unstable angina, cerebrovascular disease(except for lacunar infarction)within 6 months prior to screening visit (confirmation of eligibility) 9\. Patients with history of TIA or cerebral infarction with clear neurological symptoms 10\. Patients with peripheral arterial disease; Fontaine grade 3 or 4 11\. Patients who correspond to contraindication or careful administration of canagliflozin (except for patient under treatment of hypoglycemic agents) 12\. Patients with history of atrial fibrillation 13\. Patients who are judged as inappropriate by investigators on screening examination.

Outcomes

Primary Outcomes

Not specified

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