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
ConditionsType2 diabetes mellitus
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.
Investigators
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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