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Clinical Trial Summary

The study is a prospective, randomized controlled, double-blind study. The enrolled patients were randomly divided into two groups: the intraarticular glucose group and the intraarticular HA group.


Clinical Trial Description

The glucose group underwent 3 sessions of 6cc 25% glucose injection with a 2-week interval between each treatment. The HA group was administered intra-articular HA ((Hyruan PlusR, average MW 3000 kD; LG Life Sciences Ltd, Korea)) for sessions with a 1-week interval between each treatment. The results were measured with the visual analogue scale (VAS), Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC), and Lequesne index. A baseline for each test was measured before treatment and then the effects of the treatments were measured by each test at 6 and 12 weeks after treatment ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03690232
Study type Interventional
Source Taipei Veterans General Hospital, Taiwan
Contact Jia chi Wang, MD
Phone 886-2-28757361
Email jcwang0726@gmail.com
Status Recruiting
Phase N/A
Start date October 8, 2018
Completion date June 1, 2020

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