A clinical study for evaluating the effect of L-citrulline on physical performance
- Conditions
- one
- Registration Number
- JPRN-UMIN000014278
- Lead Sponsor
- Soiken Inc.
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- Male
- Target Recruitment
- 20
Not provided
1) Subject taking any medical treatment(prescribed a medicine by a doctor) 2) Subject receiving a medical treatment for serious renal, hepatic, cardio-vascular, respiratory, endocrine or metabolic disorders or having a medical history of these disorders 3) Subject having a medical history of a chest pain or swoon career 4) Subject having a subjective symptom of low back pain, arthralgia or lumber hernia, disease of lower limbs, palpitations 5) Subject having an abnormality in the electrocardiogram 6) Subject having the possibilty of developing allergic symptoms by test food 7) Subject having blood sample of 200 ml or more taken (e.g., donated blood) within 1 month, or 400 ml or more within 3 months prior to the start of the present study 8) Subject having the habit of taking a supplement 9) Subject received a serious injury within past 1 year 10) Subject taking part in any sports events during the present study period or within 1 month before and after the period 11) Subject going abroad or having a trip for more than 3 days and 2 nights during the present study 12) Subject having a smoking habit 13) Subject having a seasonal allergy of a cedar or Japanese cypress pollen 14) Subject who took part in another clinical trial within 3 months prior to the start of the present study or who is currently taking part in another clinical trial 15) Subject judged to be ineligible by the investigator for other reason
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 4km cycling time trial performance
- Secondary Outcome Measures
Name Time Method bloodchemisty(NOx), VO2 and visual analogue scale