Trials / Enrolling By Invitation
Enrolling By InvitationNCT05916092
Post-Market Clinical Study on a Modular SI Joint Fusion System
A Prospective, Multicenter, Post Market Surveillance Study on a Modular SI Joint Fusion System
- Status
- Enrolling By Invitation
- Phase
- —
- Study type
- Observational
- Enrollment
- 240 (estimated)
- Sponsor
- CornerLoc · Industry
- Sex
- All
- Age
- 18 Years – 85 Years
- Healthy volunteers
- Not accepted
Summary
A prospective study on the use of the TransLoc 3D SI Joint Fusion System for patients with sacroiliac joint disruptions or degenerative sacroiliitis.
Detailed description
Multicenter, prospective, post-market surveillance study on the TransLoc 3D Sacroiliac Joint Fusion System including two treatment arms: 1) Lateral-Oblique TransLoc 3D Screw(s), 2) Lateral Oblique TransLoc 3D Screw with Posterior Device (Hybrid). Data from this post-market study will be used to support knowledge of clinical efficacy and improvement with the use of TransLoc 3D Sacroiliac Joint Fusion System.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | TransLoc 3D | TransLoc 3D SI Joint Fusion System |
Timeline
- Start date
- 2023-10-19
- Primary completion
- 2025-12-01
- Completion
- 2026-07-01
- First posted
- 2023-06-23
- Last updated
- 2024-02-06
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT05916092. Inclusion in this directory is not an endorsement.