Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Jacquet-Guibon, Sandrine, Dupays, Anne-Gaelle, Coudry, Virginie, Crevier-Denoix, Nathalie, Leroy, Sandrine, Siñeriz, Fernando, Chiappini, Franck, Barritault, Denis, Denoix, Jean-Marie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
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
Descripción
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.