Real-World Registry Study on Patient Satisfaction With TransLoc 3D SI Joint Fusion
NCT06487936 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 120
Last updated 2024-08-23
Summary
This is a multi-center, consecutive enrollment registry study to evaluate patient satisfaction post SI Fusion with the TransLoc 3D SI Fusion System.
Conditions
- Sacroiliac Joint Dysfunction
- Sacroiliac; Fusion
Interventions
- DEVICE
-
TransLoc 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.
Sponsors & Collaborators
-
CornerLoc
lead INDUSTRY
Principal Investigators
-
Lee James, DO · Advanced Orthopedic Center
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2024-08-15
- Primary Completion
- 2024-10-15
- Completion
- 2024-12-15
- FDA Device
- Yes
Countries
- United States
Study Locations
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