Condition: Idiopathic Scoliosis · Sponsor: Globus Medical Inc
The purpose of this multi-center, prospective, single-arm registry Post-Approval Study (PAS) is to evaluate the radiographic and clinical outcomes of 100 patients with idiopathic scoliosis treated with the REFLECT™ Scoliosis Correction System, as a condition of HDE approval
This description comes directly from the study's public registry record.
Rebecca Smith · 858-922-7112 · rsmith@globusmedical.com
Shannon Bahn · sbahn@globusmedical.com
Always discuss trial participation with your own doctor first.
| Mayo Clinic | Rochester, Minnesota, United States | Recruiting |
| New York University | New York, New York, United States | Enrolling By Invitation |
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Source record: clinicaltrials.gov/study/NCT06298812