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A Multicentric, Open-Label, Randomized, Comparative Clinical Trial of Two Different Doses of Expanded hBM-MSCs Plus Biomaterial versus Iliac Crest Autograft, for Bone Healing in Nonunions after Long Bone Fractures: Study Protocol

Authors :
Enrique Gómez-Barrena
Norma G. Padilla-Eguiluz
Cristina Avendaño-Solá
Concepción Payares-Herrera
Ana Velasco-Iglesias
Ferran Torres
Philippe Rosset
Florian Gebhard
Nicola Baldini
Juan C. Rubio-Suarez
Eduardo García-Rey
José Cordero-Ampuero
Javier Vaquero-Martin
Francisco Chana
Fernando Marco
Javier García-Coiradas
Pedro Caba-Dessoux
Pablo de la Cuadra
Philippe Hernigou
Charles-Henri Flouzat-Lachaniette
François Gouin
Didier Mainard
Jean Michel Laffosse
Miriam Kalbitz
Ingo Marzi
Norbert Südkamp
Ulrich Stöckle
Gabriela Ciapetti
Davide Maria Donati
Luigi Zagra
Ugo Pazzaglia
Guido Zarattini
Rodolfo Capanna
Fabio Catani
Source :
Stem Cells International, Vol 2018 (2018)
Publication Year :
2018
Publisher :
Hindawi Limited, 2018.

Abstract

ORTHOUNION is a multicentre, open, comparative, three-arm, randomized clinical trial (EudraCT number 2015-000431-32) to compare the efficacy, at one and two years, of autologous human bone marrow-derived expanded mesenchymal stromal cell (hBM-MSC) treatments versus iliac crest autograft (ICA) to enhance bone healing in patients with diaphyseal and/or metaphysodiaphyseal fracture (femur, tibia, and humerus) status of atrophic or oligotrophic nonunion (more than 9 months after the acute fracture, including recalcitrant cases after failed treatments). The primary objective is to determine if the treatment with hBM-MSCs combined with biomaterial is superior to ICA in obtaining bone healing. If confirmed, a secondary objective is set to determine if the dose of 100 × 106 hBM-MSCs is noninferior to that of 200 × 106 hBM-MSCs. The participants (n=108) will be randomly assigned to either the experimental low dose (n=36), the experimental high dose (n=36), or the comparator arm (n=36) using a central randomization service. The trial will be conducted in 20 clinical centres in Spain, France, Germany, and Italy under the same clinical protocol. The confirmation of superiority for the proposed ATMP in nonunions may foster the future of bone regenerative medicine in this indication. On the contrary, absence of superiority may underline its limitations in clinical use.

Subjects

Subjects :
Internal medicine
RC31-1245

Details

Language :
English
ISSN :
1687966X and 16879678
Volume :
2018
Database :
Directory of Open Access Journals
Journal :
Stem Cells International
Publication Type :
Academic Journal
Accession number :
edsdoj.057c1be69d402a8b82d864767c0861
Document Type :
article
Full Text :
https://doi.org/10.1155/2018/6025918