Tier 3 — preclinical
The effects of an oral preparation containing hyaluronic acid (Oralvisc) on obese knee osteoarthritis patients determined by pain, function, bradykinin, leptin, inflammatory cytokines, and heavy water analyses
Rheumatology International
2015
35(1):43-52
Bibliography
- PubMed
- PMID 24899570
Study snapshot
| Design | Randomized, double-blind, placebo-controlled trial |
|---|---|
| Model | 40 overweight/obese adults with knee osteoarthritis |
| Sample | n=40 |
| Intervention | Oralvisc 80 mg/day, approximately 56 mg/day HA plus other glycosaminoglycans, versus placebo |
| Duration | 3 months |
| Endpoints | VAS pain; WOMAC pain and function; Inflammatory cytokines; Bradykinin; Leptin; Synovial-fluid glycosaminoglycan turnover |
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