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
Conditions
Sacroiliac Joint DysfunctionSacroiliac; Fusion
Locations
Advanced Orthopedic Center
Port Charlotte, Florida 33948
United States