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

Part of paid clinical trials in Port Charlotte, Florida.

Sponsor
CornerLoc
Study ID
NCT06487936
Status
Recruiting
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Conditions

  • Sacroiliac Joint Dysfunction
  • Sacroiliac; Fusion

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • TransLoc 3D SI Joint Fusion System — DEVICE
    Satisfaction survey will be administered to collect real world evidence on patients that previously received the TransLoc 3D System commercially.

Study Details

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

Key Dates

Start date
Aug 15, 2024
Status verified
Aug 2024
Primary completion
Oct 15, 2024
Completion
Dec 15, 2024

Study Design

Enrollment
120 participants (estimated)

Arms

  • Arm: Implanted TransLoc 3D SIJ Fusion Patients
    Patients who were diagnosed with sacroiliitis and were treated with the TransLoc 3D System ≥ 1 year ≤ 18 months at the time of consent.

Primary Outcome Measure

Patient Satisfaction Survey [ Time Frame: Prospective 12 to 18 months post surgery ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
Advanced Orthopedic CenterPort CharlotteFlorida33948
Lee James, DO

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By research site
Advanced Orthopedic Center· Port Charlotte, FL

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