Clinical Trial

REFLECT Scoliosis System Post Approval Study

Recruiting
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Summary
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
Protocol Amendment History 2 amendments
This ClinicalTrials.gov record has been amended 2 times since 2024-03-01; most recent amendment 2026-02-11.
Status change: Not Yet Recruiting → Recruiting 2025-12-15
Trial Details
NCT Number NCT06298812
Lead Sponsor Globus Medical Inc
Conditions Idiopathic Scoliosis
Enrollment 100 participants
Start Date 2024-04-08
Primary Completion 2027-03-31 (estimated)
Study Completion 2032-03-31 (estimated)
Updated on ClinicalTrials.gov 2026-02-13