JPRN-jRCT1051210063
Recruiting
未知
A Prospective Interventional Study on the Mechanism of Metformin Action Using Intestinal Mucosal Biopsy Tissue from Type 2 Diabetic Patients
Sakaguchi Kazuhiko0 sites30 target enrollmentAugust 13, 2021
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Sakaguchi Kazuhiko
- Enrollment
- 30
- Status
- Recruiting
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Metformin oral group
- •1\. patients scheduled to undergo lower gastrointestinal endoscopy
- •2\. patients with type 2 diabetes who have been taking metformin at least 1000 mg/day for more than 1 month
- •3\. patients who are expected to take no less than 1000 mg/day of metformin until they undergo lower gastrointestinal endoscopy
- •4\. patients aged 20 years or older but less than 75 years.
- •5\. patients who have given their written consent for the study.
- •Metformin non\-medication group
- •1\. patients scheduled to undergo lower gastrointestinal endoscopy
- •2\. patients with type 2 diabetes who have not taken metformin for more than 1 month.
- •3\. patients who are not expected to start metformin for a period of time before undergoing lower gastrointestinal endoscopy
Exclusion Criteria
- •1\. pregnant women, lactating women, and women who may become pregnant.
- •2\. patients with inflammatory bowel disease (Crohn's disease, ulcerative colitis) or with a history of such disease.
- •3\. patients with a history of gastrointestinal tract surgery (excluding endoscopic mucosal resection)
- •4\. patients with suspected gastrointestinal tract infections
- •5\. patients with predisposition to bleeding (platelet abnormality: von Willebrand disease, coagulation abnormality: hemophilia, vascular abnormality: IgA) Vascular abnormalities: IgA vasculitis, etc.)
- •6\. patients taking two or more anticoagulants or antiplatelet agents
- •7\. patients suffering from dementia or psychiatric disease
- •8\. patients with HBV, HCV, or HIV.
- •9\. other patients who are judged to be inappropriate by the person in charge of this study.
Outcomes
Primary Outcomes
Not specified
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