Clinical Trial of Jelly Containing the Rare Sugar D-Alulose in Patients with Type 2 Diabetes Mellitus
- Conditions
- Type 2 diabetesD-alluloseMeSH Unique ID: D003924
- Registration Number
- JPRN-jRCTs061230021
- Lead Sponsor
- Fukunaga Kensaku
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 24
1. patients with type 2 diabetes who are 20 years of age or older at the time of obtaining consent
2. patients with type 2 diabetes who are hospitalized in our hospital.
3. patients who can give written consent to participate in this study.
1. patients taking alpha-glucosidase inhibitors
2. patients who have experienced serious adverse reactions to D-alulose in the past
3. pregnant, lactating, or nursing women, or women of childbearing potential
4. patients with severe renal dysfunction (serum eGFR < 15 ml/min/1.73m2)
5. patients with other serious complications
6. patients who are participating in other studies
7. if, in the opinion of the Principal Investigator, participation in the research would not be in the best interest of the research subjects (e.g., would be detrimental to the welfare of the research subjects) or would interfere with, limit, or confound the evaluation specific to the clinical research protocol
8. an employee of the Principal Investigator or the institution, or a family member of such an employee or Principal Investigator, who is directly involved in this or other clinical research at the direction of the Principal Investigator or the institution.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method