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

Launched by CORNERLOC · Jun 27, 2024

Keywords

ClinConnect Summary

This clinical trial is studying how satisfied patients are after having surgery to treat sacroiliac joint dysfunction using a specific device called the TransLoc 3D SI Fusion System. The goal is to gather real-world feedback from patients who have received this treatment to understand their experiences and overall satisfaction.

To be eligible for the study, participants need to be at least 18 years old and must have had the TransLoc 3D Fusion System implanted. They should not have any other metal implants or have had their TransLoc device removed or replaced. Participants will need to be willing to take part in a survey about their satisfaction with the treatment and must have a follow-up CT scan planned at least one year after their surgery. If you decide to participate, you will share your experience through this survey, which will help improve future treatments for patients with similar conditions.

Gender

ALL

Eligibility criteria

• 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