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The purpose of this study is to assess the safety and fusion rates following posterior lateral fusion with the Dynesys Spinal System used as an adjunct to fusion and compare to literature control.
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Lead Sponsor
Zimmer Biomet
NCT05029726 · Lumbar Spinal Stenosis, Lumbar Disc Herniation, and more
NCT04418830 · Degenerative Disc Disease, Degenerative Spondylolisthesis, and more
NCT06000319 · Degenerative Disc Disease, Degenerative Spondylolisthesis, and more
NCT03115983 · Degenerative Spondylolisthesis, Lumbar Spinal Stenosis
NCT03562936 · Degenerative Lumbar Spinal Stenosis, Degenerative Spondylolisthesis
Neurological Surgery of Southern Ill
Belleville, Illinois
Greater Baltimore Medical Center
Baltimore, Maryland
Pine Heights Medical Center
Baltimore, Maryland
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This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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