JPRN-UMIN000027699
Completed
未知
The efficacy evaluation of the knee subjective symptoms and motor function by collagen containing drink - The efficacy evaluation of the knee subjective symptoms and motor function by collagen containing drink
TTC Co.,Ltd0 sites30 target enrollmentJune 9, 2017
ConditionsHealthy adult
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Healthy adult
- Sponsor
- TTC Co.,Ltd
- Enrollment
- 30
- Status
- Completed
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- Not provided
Exclusion Criteria
- •(1\)Subjects who exceeded the value of knee pain on JKOM, question\-I : the degree of pain, more than the sum VAS value of other joint pain (e.g., ankle, elbow, finger, shoulder, back and hip) (2\)Subjects who are confirmed 30\-points by JOA score, the degree of knee pain and walk ability (3\)Subjects who are suspected gouty attack with hyperuricemia (4\)Subjects who have positive rheumatoid factors on the screening test or may have rheumatic pain (5\)Subjects who have performed arthroplasty or need it (6\)Subjects who regularly take health food containing bone, joint, muscle wellness from three month before the screening test to the end of the study (7\)Subjects who regularly take medicine (8\)Subjects who have been performed intra\-articular hyaluronic acid or steroid drug injection within a year before the screening test (9\)Subjects who get an intense exercise to make excessive load on the joints (10\)Subjects who have a history of the disorder related to bone and joint such as fracture and sprain within a year before the screening test (11\)Subjects who regularly use a stick or supporter (12\)Subjects who routinely exert an influence on the efficacy evaluation (13\)Subjects who get a diagnosis of malignancy, are under treatment for hypertension, cardiac disease, renal disease and thyroid dysfunction, and have a history of serious disorder such as hepatic disease (14\)Subjects who consume an excess amounts of alcohol (15\)Subjects who have possibility of allergy symptoms onset by the test supplement (16\)Subjects who are judged as unsuitable for the study based on the results of lifestyle questionnaire (17\)Subjects who have participated in other clinical study within a month before the screening test or who intend to participate in study period (18\)Subjects who intend to become pregnant or lactating (19\)Subjects who are judged as unsuitable for this study by physician
Outcomes
Primary Outcomes
Not specified
Similar Trials
Completed
Not Applicable
Objective and subjective assessment of readiness to Return to Sport post Anterior Cruciate Ligament (ACL) reconstruction.ACTRN12617000997358Dr Matthew Liptak40
Recruiting
Not Applicable
Exploratory study on the effectiveness of the knee orthosis that prevent the inappropriate knee bending during the stance phasePatients with the inappropriate knee bending gait pattern during the stance phaseJPRN-UMIN000039220Fujita Health University50
Recruiting
Not Applicable
Investigation of the effectiveness of group exercise for people with knee paiknee osteoarthritisJPRN-UMIN000053230Saitama Prefectural University100
Completed
Not Applicable
Evaluation of the knee pain alleviating effect on the long-term intake of hyaluronic acid containing diet (Hyabest J)osteoarthritisJPRN-jRCT1090220082Kewpie Corporation60
Active, not recruiting
Not Applicable
A Clinical Investigation to evaluate the Apex KneeTM Pegged Tibial Baseplate Porous Coated components in primary Total Knee Arthroplasty using Roentgen Stereophotogrammetric Analysis (RSA)ACTRN12622000503729Corin Australia Pty Limited30