Post-op Treatment With Hyaluronic Acid Injections
Stopped early · Not applicable
Conditions studied: Meniscus Tear, Chondropathy/Degenerative Joint Disease (DJD)
In brief
This study will look at patients with post-operative treatment of a meniscal tear or degenerative joint disease (degenerative arthritis). They will be randomized into one of three groups: Euflexxa injection, saline (placebo) injection, or no injection. Those who are randomized into the injection group will receive a series of three injections (one a week for 3 weeks), then a "booster" injection at 6 months post-op. Several questionnaires will be given after the first set of injections, then again at a one year follow-up. The hypothesis is that patients receiving hyaluronic acid injections will have better pain and function scores as compared with placebo and no further treatment at all time points.
Key facts
- Study ID
- NCT01256788
- Run by
- The Hawkins Foundation
- People needed
- 34
- Starts
- 2010-09-01
- Expected to finish
- 2014-04-01
- Last updated by the study team
- 2019-01-08
Who can join
Age: 40 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patients in post-op stage of treatment for meniscal tears or chondropathy/DJD
- Over 40 years of age
- A daily knee pain above 20mm on a 100mm visual analogue scale
You may not qualify if…
- Previous recipient of viscosupplementation injections
- Had rheumatoid arthritis or other inflammatory arthritis
- Had intra-articular steroid injections within the previous 2 months
- Invasive knee procedures within the past 6 months
- Contraindications to hyaluronate (an allergy)
- Medications that could interfere with the planned interventions
Where it is running
- Steadman Hawkins Clinic of the Carolinas — Greenville, South Carolina, United States
Full record on ClinicalTrials.gov
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