The Center for Clinical Research LLC | Winston-Salem, NC
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This study is a prospective, multicenter (up to 4 sites), randomized, double-blind, two-arm study. Forty-five (45) patients will be randomized to receive a single 4-6 ml intra-articular (IA) injection of either the output of ACP Max™ (n=30) or 6 ml of Depo-Medrol® (methylprednisolone acetate) (n=15).
Full description
All subjects will have a screening visit and a treatment visit followed by six follow-up visits: 10 days, 6 weeks, 3 months, 6 months, 9 months, and 12 months.
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Interventional model
Masking
45 participants in 2 patient groups
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Central trial contact
Teresa M Reisig, MS, CCRP; Melissa Hirschberg, BSN, CCRA
Data sourced from clinicaltrials.gov
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