Fatigue recovery and exercise function improvement test
- Conditions
- ot applicable
- Registration Number
- JPRN-UMIN000051160
- Lead Sponsor
- Shonan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- Male
- Target Recruitment
- 35
Not provided
1) Subjects who are regularly taking medicines or dietary supplements that may affect the results of the study. 2) Subjects with a history or current severe heart, liver, kidney or gastrointestinal disease. 3) Subjects who drink a lot of alcohol. 4) Subjects who smoke excessively. 5) Subjects with extremely irregular eating habits, irregular rhythm of life. 6) Subjects with allergies to medicines and foods (especially gelatin) 7) Subjects who are participating the other clinical tests. Subjects who participated within 4-weeks prior to the current study and/or who plan to participate the other clinical tests. 8) Subjects who have donated component blood or 200 mL of whole blood in the month prior to study entry. 9) Subjects who have donated 400 mL of whole blood in the 3 months prior to study entry. 10) Subjects who have donated 1200 mL of whole blood in the 12 months prior to study entry. 11) Subjects deemed by principal investigator to be ineligible to participate in this study.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method