A clinical study for evaluating the effect of intake of Kefir on oral flora and intestinal flora in oral cancer patients
Not Applicable
- Conditions
- Oral cancer
- Registration Number
- JPRN-UMIN000023901
- Lead Sponsor
- Hiroshima University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up continuing
- Sex
- All
- Target Recruitment
- 45
Inclusion Criteria
Not provided
Exclusion Criteria
Patients with active double cancer. Patients with serious complications, intestinal paralysis, intestinal obstruction, interstitial pneumonia, lung fibrosis, uncontrollable diabetes, heart failure, kidney failure, liver failure. Patients with a hypersensitivity of iodinated contrast agent,milk and dairy products. Patients with severe mental disorders Patients and lactating women that might be pregnant or are pregnant Others, doctor has determined to be inappropriate as a subject of this study.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method