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Globus Reflect Tether - HUD

Globus Reflect Tether - Humanitarian Use Device

Status
Withdrawn
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06521814
Enrollment
0
Registered
2024-07-26
Start date
2025-11-01
Completion date
2025-11-01
Last updated
2025-11-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Scoliosis Idiopathic

Brief summary

The purpose of this device is to treat children and adolescents with scoliosis who have growth remaining. In patients with a curvature about the spine, Reflect holds the convexity of the curve in place so that the concavity can grow, thereby harnessing the power of normal spine growth to correct the deformity.

Detailed description

The Globus Reflect scoliosis correction system aims to provide curve correction for scoliosis patients who are still actively growing. Surgical correction is accomplished without spinal fusion, instead utilizing anterior vertebral body tethering. This device received an HDE exemption from the FDA and requires MUSC IRB approval to be used.

Interventions

(i.e. purpose of research) The Globus Reflect scoliosis correction system aims to provide curve correction for scoliosis patients who are still actively growing. Surgical correction is accomplished without spinal fusion, instead utilizing anterior vertebral body tethering. Reflect holds the convexity of the curve in place so that the concavity can grow, thereby harnessing the power of normal spine growth to correct the deformity.

Sponsors

Medical University of South Carolina
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
10 Years to 18 Years
Healthy volunteers
No

Inclusion criteria

* Skeletally immature patients that require surgical treatment to obtain and maintain correction of progressive idiopathic scoliosis, with a major Cobb angle of 35 to 60 degrees whose osseous structure is dimensionally adequate to accommodate screw fixation, as determined by radiographic imaging. * Patients should have failed bracing and/or be intolerant to brace wear.

Exclusion criteria

* Pregnancy (current) * Prior spinal or chest surgery * MRI abnormalities (including syrinx greater than 4mm, Chiari malformation, or tethered cord) * Neuromuscular, thoracogenic, cardiogenic scoliosis, or any other non-idiopathic scoliosis * Associated syndrome, including Marfan Disease or Neurofibromatosis * Sanders stage greater than 4 * Thoracic curve less than 35 or greater than 60 * Lumbar curve greater than or equal to 35 * Unable or unwilling to firmly commit to returning for required follow-up visits * Investigator judgement that the subject/family may not be a candidate for the intervention

Design outcomes

Primary

MeasureTime frameDescription
Cobb anglesUntil patients reach the age of 18Decrease in cobb angles for patients who are actively still growing

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026