A Phase 3 interventional study of Hyalgan and sterile normal saline in Osteoarthritis, sponsored by Med Pharma Co., Ltd.. Completed at 1 site in Taiwan. Open to participants aged 50 Years to 80 Years. Per ClinicalTrials.gov, last updated 2011-03-25.
Sponsored by Med Pharma Co., Ltd. · Phase 3, Interventional, and Treatment
Evaluate the efficacy and safety of Hyalgan, at a dose of 20mg/2ml administered as 5 intraarticular injections at weekly intervals, for the sustained relief of pain and amelioration of joint dysfunction in patients of OA of the knee.
4,445 studies on the registry are indexed under Osteoarthritis; 582 are open to participants now.
This study's enrollment of 200 is above the median of 70 across 3,474 interventional studies indexed under Osteoarthritis.
Browse Osteoarthritis studies →This is the only study on the registry with Med Pharma Co., Ltd. as lead sponsor.
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Exclusion Criteria:
Device: sterile normal saline
Device: Hyalgan
Patients will receive intraarticular injection of 20mg /2ml /syringe Hyalgan® once a week for 5 consecutive weeks.
Patients will receive intraarticular injection of sterile normal saline once a week for 5 consecutive weeks.
This study is completed, as verified in Mar 2011. You cannot join it, but the record below documents what was studied.
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