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NCT06487936Recruiting

Real-World Registry Study on Patient Satisfaction With TransLoc 3D SI Joint Fusion

CornerLoc

Start Date

8/15/2024

Completion Date

12/15/2024

Summary

This is a multi-center, consecutive enrollment registry study to evaluate patient satisfaction post SI Fusion with the TransLoc 3D SI Fusion System.

Eligibility Criteria

Age Range: 18 years to No maximum

Inclusion Criteria: * Age 18 year or older * Confirmed Implant of the Transloc 3D Fusion System * Did not have Transloc device removed or another manufacturer device implanted post Transloc * Does not have other manufacturer's titanium or metal implant * Patient may be included with prior allograft implant * Willing to participate and give written consent * Must have or planned CT post ≥1 year per standard of care Exclusion Criteria: * Patient is younger than 18 years * Patient is unable to sign the Informed Consent * Implant of other manufacturer's titanium or alternative metal implant * Revision with another manufacturer's implant * Fracture or unresolved trauma of implant side after implantation of TransLoc * Patient unwilling to participate in Patient Satisfaction Survey * Patient has not returned for Standard of Care follow-up

Interventions

DEVICE

TransLoc 3D SI Joint Fusion System

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Conditions

Sacroiliac Joint DysfunctionSacroiliac; Fusion

Locations

Advanced Orthopedic Center

Port Charlotte, Florida 33948

United States