Status:
RECRUITING
Real-World Registry Study on Patient Satisfaction With TransLoc 3D SI Joint Fusion
Lead Sponsor:
CornerLoc
Conditions:
Sacroiliac Joint Dysfunction
Sacroiliac; Fusion
Eligibility:
All Genders
18+ years
Brief 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
Inclusion
- 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
- 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
Key Trial Info
Start Date :
August 15 2024
Trial Type :
OBSERVATIONAL
Allocation :
ESTIMATED
End Date :
December 15 2024
Estimated Enrollment :
120 Patients enrolled
Trial Details
Trial ID
NCT06487936
Start Date
August 15 2024
End Date
December 15 2024
Last Update
August 23 2024
Active Locations (1)
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1
Advanced Orthopedic Center
Port Charlotte, Florida, United States, 33948