Healthy adults
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Healthy volunteers who give written informed consent.
Exclusion criteria
Exclusion criteria: Past gastrointestinal disorders that required in-hospital treatment Diabetes mellitus Morbid obesity (BMI>35) Pregnant woman / Breast feeding mother Orally medicated Dysphagia Diarrhea
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The gastric emptying time, the duration between ingestion of the tested solution and the time point at which the ultrasonographic cross-sectional area of the gastric antrum returns to less than +15% of the baseline value at fasting or 4 cm2. | — |
Secondary
| Measure | Time frame |
|---|---|
| Subjective impression about tested solution, the incidence of discomforts or symptom after ingestion of test solution. | — |
Countries
Japan
Contacts
Kumamoto Kinoh Hospital Division of Anesthesia