Condition: Disc Herniation · Sponsor: Columbia University
This study will be a double-blinded, two-arm, prospective, randomized controlled pilot feasibility study in 40 evaluable subjects (20 in each arm) at one study site within the United States. Subjects in Arm 1 will receive unilateral Discogen treatment; subjects in Arm 2 will receive unilateral sham treatment (control). Treatment in both arms can include medications, e.g. NSAIDs or muscle relaxants for axial or radicular pain.
This description comes directly from the study's public registry record.
Clark Smith, MD, PhD · 212-305-2134 · cs3028@cumc.columbia.edu
Michael Spinner, MS · 212-305-9416 · ms6431@cumc.columbia.edu
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| Columbia University Irving Medical Center | New York, New York, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06611397