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 …

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 …

[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 …

[HTML][HTML] Clinical study to evaluate the safety and effectiveness of the Aesculap Activ-L™ artificial disc in the treatment of degenerative disc disease

JJ Yue, FF Mo - BMC surgery, 2010 - Springer
Background The objective of this clinical study is to evaluate the safety and effectiveness of
the Activ-L Artificial Disc for treatment of single-level degenerative disc disease of the lumbar …

Clinical and radiological mid-term outcomes of lumbar single-level total disc replacement

MN Scott-Young, MJ Lee, DEA Nielsen, CL Magno… - Spine, 2018 - journals.lww.com
Study Design. Prospective single-center case cohort study. Objective. Evaluation of clinical
and radiographic outcomes of a consecutive 122-patient cohort with discogenic back pain …

[HTML][HTML] Lumbar total disc replacement for discogenic low back pain: two-year outcomes of the activL multicenter randomized controlled IDE clinical trial

R Garcia Jr, JJ Yue, S Blumenthal, D Coric, VV Patel… - 2015 - journals.lww.com
Study Design. A prospective, multicenter, randomized, controlled, investigational device
exemption (IDE) noninferiority trial. Objective. The aim of this study was to evaluate the …

[HTML][HTML] The short-term efficacy and safety of artificial total disc replacement for selected patients with lumbar degenerative disc disease compared with anterior lumbar …

X Mu, J Wei, Z Li, Y Ou - PLoS One, 2018 - journals.plos.org
Purpose To systematically compare the efficacy and safety of lumbar total disc replacement
(TDR) with the efficacy and safety of anterior lumbar interbody fusion (ALIF) for the treatment …

Clinical outcome of lumbar total disc replacement using ProDisc-L in degenerative disc disease: minimum 5-year follow-up results at a single institute

CK Park, KS Ryu, KY Lee, HJ Lee - Spine, 2012 - journals.lww.com
Study Design. A retrospective clinical data analysis. Objective. To determine the therapeutic
effectiveness of lumbar total disc replacement (TDR) using ProDisc-L (Synthes Spine, West …

[HTML][HTML] Mid-to long-term results of total disc replacement for lumbar degenerative disc disease: a systematic review

XD Cui, HT Li, W Zhang, LL Zhang, ZP Luo… - Journal of orthopaedic …, 2018 - Springer
Background Lumbar total disc replacement (TDR) has shown satisfactory clinical outcomes
with few complications and reoperations at short-term follow-up, but the mid-to long-term …

Two-to 3-year follow-up of ProDisc-L: results from a prospective randomized trial of arthroplasty versus fusion

JE Zigler, BL Sachs, RF Rashbaum, DD Ohnmeiss - SAS journal, 2007 - Elsevier
BACKGROUND: Although total disc replacement has been performed for years outside the
United States, relatively little available data address clinical outcomes, particularly data from …