RecruitingNCT06487936
Real-World Registry Study on Patient Satisfaction With TransLoc 3D SI Joint Fusion
A Multi-Center, Real World Prospective/Retrospective Registry to Evaluate Patient Satisfaction With the TransLoc 3D SI Joint Fusion System
Sponsor
CornerLoc
Enrollment
120 participants
Start Date
Aug 15, 2024
Study Type
OBSERVATIONAL
Conditions
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
Min Age: 18 Years
Inclusion Criteria7
- 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 Criteria7
- 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
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Interventions
DEVICETransLoc 3D SI Joint Fusion System
Satisfaction survey will be administered to collect real world evidence on patients that previously received the TransLoc 3D System commercially.
Locations(1)
View Full Details on ClinicalTrials.gov
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NCT06487936
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