A clinical study for evaluating the effects of P-chondroitin NHZ on knee joint symptoms
- Conditions
- Healthy volunteer
- Registration Number
- JPRN-UMIN000025992
- Lead Sponsor
- Soiken Inc.
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 40
Not provided
1)Subjects having a medical history of rheumatism 2)Subjects who have leg pain or numbness 3)Subjects who have injury of semi-lunar disc or the other knee joint disease 4) Subjects receiving treatment for osteoarthritis 5) Subject receiving treatment for serious liver, renal, cardio-vascular, respiratory, endocrine, or metabolic disorders 6) Subject presenting known allergy or history of pork 7) For female subject: pregnancy or breast feeding, or possibility of pregnancy, or intention to be pregnant during the study 8) 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 9) 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 10) Subject deemed unsuitable by the investigator
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method