Clinical performance of an elastomeric lumbar disc replacement: Minimum 12 months follow-up

L Pimenta, R Springmuller, CK Lee, L Oliveira, SE Roth… - SAS journal, 2010 - Elsevier
BACKGROUND: Elastomeric disc replacements have been developed to restore normal
shock absorption and physiologic centers of rotation to the degenerated disc. The Physio-L …

Elastomeric lumbar total disc replacement: clinical and radiological results with minimum 84 months follow-up

L Pimenta, L Marchi, L Oliveira… - International Journal of …, 2018 - ijssurgery.com
Background Total lumbar disc replacement (TDR) devices have been designed to maintain
motion, but both biomechanical and clinical data have indicated that a more controlled …

Five-year follow-up of clinical and radiological outcomes of LP-ESP elastomeric lumbar total disc replacement in active patients

JY Lazennec, JP Rakover, MA Rousseau - The Spine Journal, 2019 - Elsevier
Background context The surgical treatment of degenerative disc disease at the lumbar spine
may involve fusion. Total disc replacement (TDR) is an alternative treatment to avoid fusion …

The Viscoelastic LP-ESP Lumbar Disc Prosthesis With 6 Degrees of Freedom: A Prospective Study of 120 Patients With Two Years' Minimum Follow-Up

JY Lazennec, A Brusson, JP Rakover… - Orthopaedic …, 2013 - boneandjoint.org.uk
Introduction The viscoelastic lumbar disk prosthesis ESP is an innovative one-piece
deformable but cohesive interbody spacer; it provides 6 full degrees of freedom about the 3 …

The activL® Artificial Disc: a next-generation motion-preserving implant for chronic lumbar discogenic pain

JJ Yue, R Garcia Jr, LE Miller - Medical Devices: Evidence and …, 2016 - Taylor & Francis
Degeneration of the lumbar intervertebral discs is a leading cause of chronic low back pain
in adults. Treatment options for patients with chronic lumbar discogenic pain unresponsive …

[HTML][HTML] Five-year results of a randomized controlled trial for lumbar artificial discs in single-level degenerative disc disease

JJ Yue, R Garcia, S Blumenthal, D Coric, VV Patel… - 2019 - journals.lww.com
Study Design. A prospective, multicenter, randomized, controlled, investigational device
exemption (IDE) noninferiority trial. Objective. The aim of this study was to compare the 5 …

Preclinical and clinical experience with a viscoelastic total disc replacement

B Rischke, RS Ross, BA Jollenbeck, KB Zimmers… - SAS journal, 2011 - Elsevier
BACKGROUND: The purpose of this study is to describe the mechanical durability and the
clinical and radiographic outcomes of a viscoelastic total disc replacement (VTDR). The …

Mechanical characterization of a viscoelastic disc for lumbar total disc replacement

EC Benzel, IH Lieberman, ER Ross, RJ Linovitz… - 2011 - asmedigitalcollection.asme.org
A viscoelastic artificial disc may more closely replicate normal stiffness characteristics of the
healthy human disc compared with first-generation total disc replacement (TDR) devices …

Five-year results of a randomized controlled trial for lumbar artificial discs in single-level degenerative disc disease

JJ Yue, R Garcia - The Spine Journal, 2017 - thespinejournalonline.com
BACKGROUND CONTEXT: The activL artificial disc received Food and Drug Administration
approval in 2015 based on 2-year follow-up data. Long-term outcomes with this lumbar total …

Final long-term reporting from a randomized controlled IDE trial for lumbar artificial discs in single-level degenerative disc disease: 7-year results

K Radcliff, J Zigler, E Braxton, G Buttermann… - International Journal of …, 2021 - ijssurgery.com
Background: This study compared 7-year safety and efficacy outcomes of activL and ProDisc-
L lumbar total disc replacements in patients with symptomatic, single-level lumbar …