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Riluzole for treating spasticity in patients with chronic traumatic spinal cord injury: Study protocol in the phase ib/iib adaptive multicenter randomized controlled RILUSCI trial

BACKGROUND: Satisfactory treatment is often lacking for spasticity, a highly prevalent motor disorder in patients with spinal cord injury (SCI). Low concentrations of riluzole potently reduce the persistent sodium current, the post-SCI increase in which contributes to spasticity. The repurposing of...

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Autores principales: Cotinat, Maëva, Boquet, Isabelle, Ursino, Moreno, Brocard, Cécile, Jouve, Elisabeth, Alberti, Corinne, Bensoussan, Laurent, Viton, Jean-Michel, Brocard, Frédéric, Blin, Olivier
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9858801/
https://www.ncbi.nlm.nih.gov/pubmed/36662869
http://dx.doi.org/10.1371/journal.pone.0276892
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author Cotinat, Maëva
Boquet, Isabelle
Ursino, Moreno
Brocard, Cécile
Jouve, Elisabeth
Alberti, Corinne
Bensoussan, Laurent
Viton, Jean-Michel
Brocard, Frédéric
Blin, Olivier
author_facet Cotinat, Maëva
Boquet, Isabelle
Ursino, Moreno
Brocard, Cécile
Jouve, Elisabeth
Alberti, Corinne
Bensoussan, Laurent
Viton, Jean-Michel
Brocard, Frédéric
Blin, Olivier
author_sort Cotinat, Maëva
collection PubMed
description BACKGROUND: Satisfactory treatment is often lacking for spasticity, a highly prevalent motor disorder in patients with spinal cord injury (SCI). Low concentrations of riluzole potently reduce the persistent sodium current, the post-SCI increase in which contributes to spasticity. The repurposing of this drug may therefore constitute a useful potential therapeutic option for relieving SCI patients suffering from chronic traumatic spasticity. OBJECTIVE: RILUSCI is a phase 1b–2b trial designed to assess whether riluzole is a safe and biologically effective means of managing spasticity in adult patients with traumatic chronic SCI. METHODS: In this multicenter double-blind trial, adults (aged 18–65 years) suffering from spasticity after SCI (target enrollment: 90 participants) will be randomly assigned to be given either a placebo or a recommended daily oral dose of riluzole for two weeks. The latter dose will be previously determined in phase 1b of the study by performing double-blind dose-finding tests using a Bayesian continuous reassessment method. The primary endpoint of the trial will be an improvement in the Modified Ashworth Score (MAS) or the Numerical Rating Score (NRS) quantifying spasticity. The secondary outcomes will be based on the safety and pharmacokinetics of riluzole as well as its impact on muscle spasms, pain, bladder dysfunction and quality of life. Analyses will be performed before, during and after the treatment and the placebo-controlled period. CONCLUSION: To the best of our knowledge, this clinical trial will be the first to document the safety and efficacy of riluzole as a means of reducing spasticity in patients with chronic SCI. TRIAL REGISTRATION: The clinical trial, which is already in progress, was registered on the ClinicalTrials.gov website on August 9, 2016 under the registration number NCT02859792. TRIAL SPONSOR: Assistance Publique–Hôpitaux de Marseille.
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spelling pubmed-98588012023-01-21 Riluzole for treating spasticity in patients with chronic traumatic spinal cord injury: Study protocol in the phase ib/iib adaptive multicenter randomized controlled RILUSCI trial Cotinat, Maëva Boquet, Isabelle Ursino, Moreno Brocard, Cécile Jouve, Elisabeth Alberti, Corinne Bensoussan, Laurent Viton, Jean-Michel Brocard, Frédéric Blin, Olivier PLoS One Study Protocol BACKGROUND: Satisfactory treatment is often lacking for spasticity, a highly prevalent motor disorder in patients with spinal cord injury (SCI). Low concentrations of riluzole potently reduce the persistent sodium current, the post-SCI increase in which contributes to spasticity. The repurposing of this drug may therefore constitute a useful potential therapeutic option for relieving SCI patients suffering from chronic traumatic spasticity. OBJECTIVE: RILUSCI is a phase 1b–2b trial designed to assess whether riluzole is a safe and biologically effective means of managing spasticity in adult patients with traumatic chronic SCI. METHODS: In this multicenter double-blind trial, adults (aged 18–65 years) suffering from spasticity after SCI (target enrollment: 90 participants) will be randomly assigned to be given either a placebo or a recommended daily oral dose of riluzole for two weeks. The latter dose will be previously determined in phase 1b of the study by performing double-blind dose-finding tests using a Bayesian continuous reassessment method. The primary endpoint of the trial will be an improvement in the Modified Ashworth Score (MAS) or the Numerical Rating Score (NRS) quantifying spasticity. The secondary outcomes will be based on the safety and pharmacokinetics of riluzole as well as its impact on muscle spasms, pain, bladder dysfunction and quality of life. Analyses will be performed before, during and after the treatment and the placebo-controlled period. CONCLUSION: To the best of our knowledge, this clinical trial will be the first to document the safety and efficacy of riluzole as a means of reducing spasticity in patients with chronic SCI. TRIAL REGISTRATION: The clinical trial, which is already in progress, was registered on the ClinicalTrials.gov website on August 9, 2016 under the registration number NCT02859792. TRIAL SPONSOR: Assistance Publique–Hôpitaux de Marseille. Public Library of Science 2023-01-20 /pmc/articles/PMC9858801/ /pubmed/36662869 http://dx.doi.org/10.1371/journal.pone.0276892 Text en © 2023 Cotinat et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Study Protocol
Cotinat, Maëva
Boquet, Isabelle
Ursino, Moreno
Brocard, Cécile
Jouve, Elisabeth
Alberti, Corinne
Bensoussan, Laurent
Viton, Jean-Michel
Brocard, Frédéric
Blin, Olivier
Riluzole for treating spasticity in patients with chronic traumatic spinal cord injury: Study protocol in the phase ib/iib adaptive multicenter randomized controlled RILUSCI trial
title Riluzole for treating spasticity in patients with chronic traumatic spinal cord injury: Study protocol in the phase ib/iib adaptive multicenter randomized controlled RILUSCI trial
title_full Riluzole for treating spasticity in patients with chronic traumatic spinal cord injury: Study protocol in the phase ib/iib adaptive multicenter randomized controlled RILUSCI trial
title_fullStr Riluzole for treating spasticity in patients with chronic traumatic spinal cord injury: Study protocol in the phase ib/iib adaptive multicenter randomized controlled RILUSCI trial
title_full_unstemmed Riluzole for treating spasticity in patients with chronic traumatic spinal cord injury: Study protocol in the phase ib/iib adaptive multicenter randomized controlled RILUSCI trial
title_short Riluzole for treating spasticity in patients with chronic traumatic spinal cord injury: Study protocol in the phase ib/iib adaptive multicenter randomized controlled RILUSCI trial
title_sort riluzole for treating spasticity in patients with chronic traumatic spinal cord injury: study protocol in the phase ib/iib adaptive multicenter randomized controlled rilusci trial
topic Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9858801/
https://www.ncbi.nlm.nih.gov/pubmed/36662869
http://dx.doi.org/10.1371/journal.pone.0276892
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