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)

Advanced Orthopedic Center

Port Charlotte, Florida, United States

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NCT06487936


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