Efficacy evaluation of PC-VIPR for the hemodynamic assessment of intestinal tract by using daikenchuto (TU-100)
Not Applicable
- Conditions
- Healthy volunteers
- Registration Number
- JPRN-UMIN000027472
- Lead Sponsor
- Hamamatsu University School of Medicine
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 20
Inclusion Criteria
Not provided
Exclusion Criteria
1. Person with MRI contraindications (claustrophobic, metal in the body, etc.) 2.High blood pressure 3.The past of the heart disease 4.With the history of abdominal surgery 5.Under the medical treatment 6.Disable to keep face up position 7.Pregnant or possibly pregnant 8.Under the nursing
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Ratio of SMA flow volume at t=25 min to t=-25 min measured by US and PC-VIPR.
- Secondary Outcome Measures
Name Time Method