None listed
Conditions
Interventions
Dietary Supplement : At Visit 1 (Week -2), volunteers who voluntarily sign the informed consent form for the human application study will be assessed for eligibility based on the inclusion and exclusi
Sponsors
Global Medical Research Center
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1) Those who agreed to participate in this study and signed a written informed consent 2) Adults (Age=19 years and =70 years) 3) Fasting blood glucose=100 mg/dL and <140 mg/dL (If values fall outside the criteria, retesting may be conducted considering measurement error and daily variation)"
Exclusion criteria
Exclusion criteria: 1) Current use of antidiabetic medication or requirement for antidiabetic treatment (HbA1c =6.5%). 2) Continuous use of medications, herbal remedies, or dietary supplements affecting glucose metabolism within one month prior to the first visit. 3) Presence of any of the following conditions: heart failure, coronary artery disease, uncontrolled hypertension, hyperlipidemia, renal dysfunction, liver dysfunction, thyroid disorders, chronic gastrointestinal disorders, history of gastrointestinal surgery, acute or chronic inflammatory diseases, malignancies, or psychiatric disorders. 4) Body mass index (BMI) =18.5 kg/m² or =30 kg/m². etc
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| glucose;insulin;appeitie VAS;Glycated hemoglobin (HbA1c) | — |
Secondary
| Measure | Time frame |
|---|---|
| Vital sign;Clinical laboratory test(blood, urine);Adverse event | — |
Countries
Korea, Republic of
Contacts
Public ContactInah Kim
Global Medical Research Center
Outcome results
None listed