Knee injection
ProcedureInjection into knee for the treatment of Osteoarthritis
NCT Number: NCT02318511
This is a Prospective, Randomized study evaluating the efficacy of ReNu for the treatment of Kellgren-Lawrence grade 2 or 3 osteoarthritis. Patients will be randomized into 1 of 3 groups for injection into the effected knee: 1) ReNu - study treatment, 2) Hyaluronic Acid (HA) injection - with commonly used injection material and 3) Saline. After treatment, patients will be followed up to 12 months to evaluate improvements using common pain and function subscales.
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Notify Me18 year and older
All sexes
Interventional
Not applicable
American Sports Medicine Institute, Birmingham, Alabama, United States
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Injection into knee for the treatment of Osteoarthritis
Time frame: 3 months
Time frame: 6 months
Time frame: 3 months
Time frame: 6 months
Time frame: 1 week, 6 weeks, 3 months, and 12 months
Time frame: 1 week, 6 week, 3 months, 6 months, and 12 months
Time frame: 12 months
NuTech Medical, Inc
Industry
An Investigation of ReNu™ Knee Injection: Monitoring the Response of Knee Function and Pain in Patients With Osteoarthritis
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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