Clinical study with healthy volunteer to measure the volume of gastric fluid after oral drug administratio
- Conditions
- digestive disorder
- Registration Number
- JPRN-UMIN000002860
- Lead Sponsor
- Faculty of Pharmaceutical Sciences, Setsunan University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Male
- Target Recruitment
- 8
Not provided
1)Who having (or had) a medical history of circulatory system disease, hepatic disease, renal disease, digestive system disease, hematological disorder. 2)Who taking a medicine that night affect the study result. 3)Who judged as inappropriate to this study by the primary doctor of this study from diagnosis, vital signs, inductive electrocardiograph, hematological assessment, blood biochemical test, urinary test, immunological test. 4)Who took a medicine within 7 days before the study 5)Who participated in the clinical trail and took a test medicine within 3 months before the study. 6)Who having (or had) an allergic constitution to medicine/food 7)Who having (or had) a dependency to drug or alcohol 8)Who judged as inappropriate to this study by the primary doctor due to any other reasons
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Time-course of drug concentration in the gastric fluid (for 3 hours after oral administration)
- Secondary Outcome Measures
Name Time Method