Trials / Unknown
UnknownNCT05633888
Post-Market Feasibility Study of the Tenon Medical CATAMARAN™ SI Joint Fusion System
Prospective, Multi-Center, Single Arm Post-Market Feasibility Study of the Tenon Medical CATAMARAN™ SI Joint Fusion System
- Status
- Unknown
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 50 (estimated)
- Sponsor
- Tenon Medical · Industry
- Sex
- All
- Age
- 18 Years – 75 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to evaluate the outcomes of patients with sacroiliac joint pain treated with the CATAMARAN SI Joint Fusion System.
Detailed description
This is a multi-center post-market study to evaluate the clinical outcomes of patients with sacroiliac joint disruptions or degenerative sacroiliitis treated with the CATAMARAN SI Joint Fusion System.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | CATAMARAN SI Joint Fusion System | Placement of the Catamaran Fixation Device |
Timeline
- Start date
- 2022-11-14
- Primary completion
- 2025-01-01
- Completion
- 2026-01-01
- First posted
- 2022-12-01
- Last updated
- 2024-03-20
Locations
6 sites across 1 country: United States
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT05633888. Inclusion in this directory is not an endorsement.