Comprehensive Observational and Longitudinal study on the Outbreak of Stroke-related Spasticity focusing on the Early Onset management with Botulinum NeuroToxin (COLOSSEO-BoNT): protocol for a real-world prospective observational study on upper limb spasticity.
Clinical trials
NEUROLOGY
PAIN MANAGEMENT
Quality of Life
REHABILITATION MEDICINE
STROKE MEDICINE
Journal
BMJ open
ISSN: 2044-6055
Titre abrégé: BMJ Open
Pays: England
ID NLM: 101552874
Informations de publication
Date de publication:
01 Jul 2024
01 Jul 2024
Historique:
medline:
2
7
2024
pubmed:
2
7
2024
entrez:
1
7
2024
Statut:
epublish
Résumé
Poststroke spasticity (PSS) affects up to 40% of patients who had a stroke. Botulinum neurotoxin type A (BoNT-A) has been shown to improve spasticity, but the optimal timing of its application remains unclear. While several predictors of upper limb PSS are known, their utility in clinical practice in relation to BoNT-A treatment has yet to be fully elucidated. The COLOSSEO-BoNT study aims to investigate predictors of PSS and the effects of BoNT-A timing on spasticity-related metrics in a real-world setting. The recruitment will involve approximately 960 patients who have recently experienced an ischaemic stroke (within 10 days, V0) and will follow them up for 24 months. Parameters will be gathered at specific intervals: (V1) 4, (V2) 8, (V3) 12, (V4) 18 months and (V5) 24 months following enrolment. Patients will be monitored throughout their rehabilitation and outpatient clinic journeys and will be compared based on their BoNT-A treatment status-distinguishing between patients receiving treatment at different timings and those who undergo rehabilitation without treatment. Potential predictors will encompass the Fugl-Meyer assessment, the National Institute of Health Stroke Scale (NIHSS), stroke radiological characteristics, performance status, therapies and access to patient care pathways. Outcomes will evaluate muscle stiffness using the modified Ashworth scale and passive range of motion, along with measures of quality of life, pain, and functionality. This study underwent review and approval by the Ethics Committee of the Fondazione Policlinico Universitario Campus Bio-Medico, Rome, Italy. Regardless of the outcome, the findings will be disseminated through publication in peer-reviewed journals and presentations at national and international conferences. NCT05379413.
Identifiants
pubmed: 38950995
pii: bmjopen-2024-085484
doi: 10.1136/bmjopen-2024-085484
doi:
Substances chimiques
Botulinum Toxins, Type A
EC 3.4.24.69
Neuromuscular Agents
0
Banques de données
ClinicalTrials.gov
['NCT05379413']
Types de publication
Journal Article
Observational Study
Clinical Trial Protocol
Langues
eng
Sous-ensembles de citation
IM
Pagination
e085484Investigateurs
Alessandro Magliozzi
(A)
Stefano Toro
(S)
Gaia Anzini
(G)
Claudia Celletti
(C)
Marco Andrighetti
(M)
Paolo Amisano
(P)
Marco Falletti
(M)
Marina Diomedi
(M)
Pierandrea Rizzo
(P)
Luigi Polidori
(L)
Grazia Libutti
(G)
Marilena Mangiardi
(M)
Francesca Romana Pezzella
(FR)
Silvia La Cesa
(S)
Claudio Gasperini
(C)
Marina Cao
(M)
Francesco Asci
(F)
Serena Capobianco
(S)
Luisella D'Angeli
(L)
Caterina Galluccio
(C)
Deepak Gupta
(D)
Informations de copyright
© Author(s) (or their employer(s)) 2024. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.
Déclaration de conflit d'intérêts
Competing interests: None declared.