Effect of Imeglimin on muscle sympathetic nerve activiy in type 2 diabetes mellitus patients
- Conditions
- Type 2 diabetesType 2 diabetes, muscle sympathetic nerve activityD003924
- Registration Number
- JPRN-jRCT1041220023
- Lead Sponsor
- Takamura Masayuki
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Not specified
- Target Recruitment
- 30
1) Age 20 to 80 years old
2) Patients diagnosed with type 2 diabetes
3) HbA1c> 7% and <10% patients
4) Patients who received sufficient explanation before participating in this study, and who obtained the patient's free will to consent to the document after sufficient understanding.
1) Patients with a history of stroke or vascular replacement surgery
2) Patients who develop myocardial infarction within 3 months
3) Patients with acute coronary syndrome
4) Patients receiving drug therapy for serious lung diseases such as interstitial pneumonia
5) Patients with organic heart disease such as severe valvular disease and shunt disease
6) Patients with moderate renal dysfunction (eGFR<45 ml / min / 1.73 m2) or hepatic dysfunction (PT activity <80%)
7) Patients suspected of being involved in secondary diabetes (endocrine, drug-induced, cirrhosis, e
tc.)
8) Compromised patients such as immunocompromised patients
9) Patients with a history or complication of ketoacidosis, diabetic coma or precoma
10) Patients with a history of severe hypoglycemic symptoms with coma or loss of consciousness, or
patients with hypoglycemic symptoms (more than twice a week) in the last 8 weeks
11) Patients suspected of alcohol or substance abuse
12) Pregnant or potentially pregnant patients, or lactating patients
13) Patients being treated for malignant tumors
14) Patients with a history of hypersensitivity to imeglimin hydrochloride
15) Patients participating in other clinical trials
16) Other patients who are judged by the investigator (sharing) to be inappropriate as subjects
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method