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Clinical Trial of Jelly Containing the Rare Sugar D-Alulose in Patients with Type 2 Diabetes Mellitus

Not Applicable
Recruiting
Conditions
Type 2 diabetes
D-allulose
MeSH 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
Inclusion Criteria

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.

Exclusion Criteria

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
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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