A double-blind, placebo controlled, randomized trial to evaluate the efficacy of SE in post-stroke rehabilitation patients.
Not Applicable
- Conditions
- Stroke
- Registration Number
- JPRN-UMIN000012902
- Lead Sponsor
- Tokyo Bay Rehabilitation Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 40
Inclusion Criteria
Not provided
Exclusion Criteria
1. Impossible to get informed concent by cognitive deficit 2. Impossible to be treated with exercise therapy due to complication or previous disease 3. Impossible to swallow experimental food 4. Patients who receive parenteral or enteral Nutrition 5. peel of citrus species supplementation 6. Patients who are judged inappropriate for the study by the physician
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method