Post-Market Feasibility Study of the Tenon Medical CATAMARAN™ SI Joint Fusion System
NCT05633888 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 50
Last updated 2024-03-20
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.
Conditions
- Sacroiliac Joint Disruption
- Degenerative Sacroiliitis
Interventions
- DEVICE
-
CATAMARAN SI Joint Fusion System
Placement of the Catamaran Fixation Device
Sponsors & Collaborators
-
Tenon Medical
lead INDUSTRY
Study Design
- Allocation
- NA
- Purpose
- OTHER
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Max Age
- 75 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2022-11-14
- Primary Completion
- 2025-01-31
- Completion
- 2026-01-31
- FDA Device
- Yes
Countries
- United States
Study Locations
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