Healty volunteers
Conditions
Interventions
The two groups cross-over study
1 first visit: Pre-sleeving examination (observation of blood sugar level after meal load) 2 visits to the 2nd and third visits: Single intake of test food or placebo
Sponsors
P-One Clinic, Keikokai Medical Corporation.
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1.The person who does not treat the disease 2.Adult aged from 20y to 60y,both sexes,The person who participates voluntarily 3.Subject whose BMI is 18.5 kg/m2 or more and less than 25 kg/m2 4.Subjects with fasting bllod glucose level under 125mg/dl 5.The person who is relatively high in blood sugar level after a meal at the time of the prior screening examination 6.Serious disease (mental diseases such as diabetes, a heart trouble, a liver disease, renal disease, a malignant tumor and the depression) without the anamnesis 7.The person who can maintain an everyday lifestyle during testing period constantly"
Exclusion criteria
Exclusion criteria: 1.Person with a history of the past who treat a serious disease (mental diseases such as diabetes, a heart trouble, a liver disease, renal disease, a malignant tumor and the depression) 2.more than 6.5% of hemoglobin A1c (NGSP) 3.After a meal the blood sugar level of 120 minutes more than 200 mg/dL 4.The person whom alimentary system such as gastric resection has in an operation career 5.The person who cannot maintain an everyday lifestyle constantly 6.Person with the shift work, person with the graveyard shift 7.Food allergy for the test food, the drug allergy which are thought about 8.A pregnant woman, nursing girl and the person who hope for the pregnancy all over the study time 9.Paticipants in other clinical trial 10.Volunteers rejected participanting in this study by chif investigator"
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| postprandial blood glucose level(AUC) | — |
Countries
Japan
Contacts
Public ContactTatsuo Uetake
CXwellness, Inc. CEO
Outcome results
None listed