RecruitingNot Applicable

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

United States120 participantsStarted 2024-08-15

Plain-language summary

This is a multi-center, consecutive enrollment registry study to evaluate patient satisfaction post SI Fusion with the TransLoc 3D SI Fusion System.

Who can participate

Age range

18 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

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

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

Patient Satisfaction Survey

Timeframe: Prospective 12 to 18 months post surgery

Trial details

NCT IDNCT06487936

SponsorCornerLoc

Sponsor typeINDUSTRY

Study typeOBSERVATIONAL

Primary completion2024-10-15

Contact for this trial

Carley Wiegner

888-743-8736 carley@cornerloc.com

View on ClinicalTrials.gov More Sacroiliac Joint Dysfunction trials

Who can participate

Age range

18 Years

Sex

ALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.