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Randomized controlled trial demonstrates the benefit of RGTA(®) based matrix therapy to treat tendinopathies in racing horses
A randomized controlled trial was performed on racing horses, to evaluate the efficacy of a new class of therapeutic agents in regenerative medicine—ReGeneraTing Agents(®) (RGTA(®)), to treat tendinopathies. Preliminary uncontrolled studies on tendon healing in racing horses with RGTA(®) (OTR4131)—E...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5844532/ https://www.ncbi.nlm.nih.gov/pubmed/29522564 http://dx.doi.org/10.1371/journal.pone.0191796 |
Sumario: | A randomized controlled trial was performed on racing horses, to evaluate the efficacy of a new class of therapeutic agents in regenerative medicine—ReGeneraTing Agents(®) (RGTA(®)), to treat tendinopathies. Preliminary uncontrolled studies on tendon healing in racing horses with RGTA(®) (OTR4131)—Equitend(®) showed encouraging results, justifying performing a randomized, controlled, multicenter study with a two-year racing performance follow up. The objective of this study was to evaluate the effect of Equitend(®) versus placebo on acute superficial digital flexor tendonitis in racing French Standardbred Trotters (ST). Twenty-two ST were randomly and blindly assigned to receive with a ratio of 2 to 1, a single Equitend(®) (n = 14) or placebo (n = 8) intralesional injection under ultrasonographic guidance. Horses were evaluated over 4 months, by clinical and ultrasonographic evaluations (day 0, months 1, 2, 4), and their racing performances followed up over the 2 years after treatment. During the first month of treatment, a significant decrease in the cross-sectional area (CSA) was found in the Equitend(®) group (p = 0.04). After 4 months, the number of Equitend(®) treated horses with an improved CSA was significantly higher than the placebo-treated horses (p = 0.03571). The Equitend(®) group returned to their pre-injury performance level, racing in, and winning, significantly more races than the placebo group (p = 0.01399 and 0.0421, respectively). Furthermore, recurrence was significantly higher in the placebo group than in the Equitend(®) group (71.4% vs 16.6%, p = 0.02442). In conclusion, we measured a significant, short-term, reduction effect on CSA and demonstrated a long-term beneficial effect of intralesional injection of Equitend(®) for the treatment of superficial digital flexor tendonitis on racing ST, racing 2. 3 times more often than placebo, with 3.3 times fewer recurrences maintaining pre-injury performance level. This study may open the way for the development of a human treatment of tendonitis. |
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