None
Conditions
Interventions
Tagatose preload group:Consuming tagatose 20 minutes before a standardized breakfast comprising white bread and butter
Co-ingestion of tagatose group:Consuming tagatose with a standardized breakfast consisting of white bread and butter
Control group:Consuming glucose with a standardized breakfast consisting of white bread and butter
Sponsors
China Agricultural University
Eligibility
Sex/Gender
All
Age
18 Years to 60 Years
Inclusion criteria
Inclusion criteria: 1. Age>=18 years; 2. No history of food allergies; 3. Able to tolerate fasting for at least 10h; 4. People with normal blood sugar or prediabetes; 5. Voluntarily participate in this trial and sign the informed consent form.
Exclusion criteria
Exclusion criteria: 1. Pregnant women, nursing mothers, patients with tumors and other major diseases; 2. Severe mental illness, such as schizophrenia; 3. Have a history of food allergies; 4. Have a history of diabetes mellitus or have genetic syndromes or diseases known to affect glucose tolerance (such as glucose-6-phosphate dehydrogenase deficiency, polycystic ovary syndrome, etc.); 5. Taking drugs known to affect glucose tolerance (such as thiazide diuretics, glucocorticoids, spironolactone, etc.) in the past 1 month; 6. In the past 1 month, there have been drugs that affect appetite and gastrointestinal function; 7. Have taken antibiotics and probiotics in the past 1 month; 8. Those who are losing weight; 9. Smokers and alcoholics; 10. Those who participate in other clinical trials; 11. Those who are not proficient in operating smartphones; 12. Wearing a continuous glucose meter is not accepted.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Blood glucose; | — |
Secondary
| Measure | Time frame |
|---|---|
| Satiety/Appetite score;Adverse event; | — |
Countries
China
Contacts
Public ContactRuixin Zhu
China Agricultural University
Outcome results
None listed