The effect of extracorporeal shock wave therapy in acute traumatic spinal cord injury on motor and sensory function within 6 months post-injury: a study protocol for a two-arm three-stage adaptive, prospective, multi-center, randomized, blinded, placebo-controlled clinical trial.


Journal

Trials
ISSN: 1745-6215
Titre abrégé: Trials
Pays: England
ID NLM: 101263253

Informations de publication

Date de publication:
01 Apr 2022
Historique:
received: 11 03 2021
accepted: 07 03 2022
entrez: 2 4 2022
pubmed: 3 4 2022
medline: 6 4 2022
Statut: epublish

Résumé

The pathological mechanism in acute spinal cord injury (SCI) is dual sequential: the primary mechanical lesion and the secondary injury due to a cascade of biochemical and pathological changes initiated by the primary lesion. Therapeutic approaches have focused on modulating the mechanisms of secondary injury. Despite extensive efforts in the treatment of SCI, there is yet no causal, curative treatment approach available. Extracorporeal shock wave therapy (ESWT) has been successfully implemented in clinical use. Biological responses to therapeutic shock waves include altered metabolic activity of various cell types due to direct and indirect mechanotransduction leading to improved migration, proliferation, chemotaxis, modulation of the inflammatory response, angiogenesis, and neovascularization, thus inducing rather a regeneration than repair. The aim of this clinical study is to investigate the effect of ESWT in humans within the first 48 h after an acute traumatic SCI, with the objective to intervene in the secondary injury phase in order to reduce the extent of neuronal loss. This two-arm three-stage adaptive, prospective, multi-center, randomized, blinded, placebo-controlled study has been initiated in July 2020, and a total of 82 patients with acute traumatic SCI will be recruited for the first stage in 15 participating hospitals as part of a two-armed three-stage adaptive trial design. The focused ESWT (energy flux density: 0.1-0.19 mJ/mm The application of ESWT activates the nervous tissue regeneration involving a multitude of various biochemical and cellular events and leads to a decreased neuronal loss. ESWT might contribute to an improvement in the treatment of acute traumatic SCI in future clinical use. ClinicalTrials.gov NCT04474106.

Sections du résumé

BACKGROUND BACKGROUND
The pathological mechanism in acute spinal cord injury (SCI) is dual sequential: the primary mechanical lesion and the secondary injury due to a cascade of biochemical and pathological changes initiated by the primary lesion. Therapeutic approaches have focused on modulating the mechanisms of secondary injury. Despite extensive efforts in the treatment of SCI, there is yet no causal, curative treatment approach available. Extracorporeal shock wave therapy (ESWT) has been successfully implemented in clinical use. Biological responses to therapeutic shock waves include altered metabolic activity of various cell types due to direct and indirect mechanotransduction leading to improved migration, proliferation, chemotaxis, modulation of the inflammatory response, angiogenesis, and neovascularization, thus inducing rather a regeneration than repair. The aim of this clinical study is to investigate the effect of ESWT in humans within the first 48 h after an acute traumatic SCI, with the objective to intervene in the secondary injury phase in order to reduce the extent of neuronal loss.
METHODS METHODS
This two-arm three-stage adaptive, prospective, multi-center, randomized, blinded, placebo-controlled study has been initiated in July 2020, and a total of 82 patients with acute traumatic SCI will be recruited for the first stage in 15 participating hospitals as part of a two-armed three-stage adaptive trial design. The focused ESWT (energy flux density: 0.1-0.19 mJ/mm
DISCUSSION CONCLUSIONS
The application of ESWT activates the nervous tissue regeneration involving a multitude of various biochemical and cellular events and leads to a decreased neuronal loss. ESWT might contribute to an improvement in the treatment of acute traumatic SCI in future clinical use.
TRIAL REGISTRATION BACKGROUND
ClinicalTrials.gov NCT04474106.

Identifiants

pubmed: 35365190
doi: 10.1186/s13063-022-06161-8
pii: 10.1186/s13063-022-06161-8
pmc: PMC8973563
doi:

Banques de données

ClinicalTrials.gov
['NCT04474106']

Types de publication

Clinical Trial Protocol Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

245

Subventions

Organisme : Allgemeine Unfallversicherungsanstalt
ID : NA

Informations de copyright

© 2022. The Author(s).

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Auteurs

Iris Leister (I)

ParaMove, SCI Research Unit, BG Trauma Center Murnau, Murnau, Germany, and Paracelus Medical University, Salzburg, Austria. iris.leister@bgu-murnau.de.
Spinal Cord Injury Center, Clinical Research Unit, BG Trauma Center Murnau, Murnau, Germany. iris.leister@bgu-murnau.de.
Institute of Molecular Regenerative Medicine, Paracelsus Medical University, Salzburg, Austria. iris.leister@bgu-murnau.de.
Spinal Cord Injury and Tissue Regeneration Center Salzburg (SCI-TReCS), Paracelsus Medical University, Salzburg, Austria. iris.leister@bgu-murnau.de.

Rainer Mittermayr (R)

Ludwig-Boltzmann Institute for Experimental and Clinical Traumatology, Vienna, Austria.
AUVA Trauma Center Meidling, Vienna, Austria.

Georg Mattiassich (G)

Ludwig-Boltzmann Institute for Experimental and Clinical Traumatology, Vienna, Austria.
Department of Orthopedics and Trauma Surgery, Klinik Diakonissen Schladming, Schladming, Austria.

Ludwig Aigner (L)

ParaMove, SCI Research Unit, BG Trauma Center Murnau, Murnau, Germany, and Paracelus Medical University, Salzburg, Austria.
Institute of Molecular Regenerative Medicine, Paracelsus Medical University, Salzburg, Austria.
Spinal Cord Injury and Tissue Regeneration Center Salzburg (SCI-TReCS), Paracelsus Medical University, Salzburg, Austria.

Thomas Haider (T)

Department of Orthopedics and Trauma Surgery, Medical University of Vienna, Vienna, Austria.

Lukas Machegger (L)

Division of Neuroradiology, Christian Doppler Medical Center, Paracelsus Medical University, Salzburg, Austria.

Harald Kindermann (H)

Department of Marketing and Electronic Business, University of Applied Sciences Upper Austria, Steyr, Austria.

Anja Grazer-Horacek (A)

AUVA Rehabilitation Clinic Tobelbad, Tobelbad, Austria.

Johannes Holfeld (J)

University Clinic of Cardiac Surgery, Medical University of Innsbruck, Innsbruck, Austria.

Wolfgang Schaden (W)

Ludwig-Boltzmann Institute for Experimental and Clinical Traumatology, Vienna, Austria.
AUVA Trauma Center Meidling, Vienna, Austria.

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