Post-Market Feasibility Study of the Tenon Medical CATAMARAN™ SI Joint Fusion System

Sacroiliac Joint Disruption Clinical Trial

Official title:
Prospective, Multi-Center, Single Arm Post-Market Feasibility Study of the Tenon Medical CATAMARAN™ SI Joint Fusion System

Status Recruiting

Clinical Trial 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.

Clinical Trial 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. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT05633888
Study type	Interventional
Source	Tenon Medical
Contact	Calvin Lincé
Phone	(510)274-7483
Email	clince@linceconsulting.com
Status	Recruiting
Phase	N/A
Start date	November 14, 2022
Completion date	January 2026

View Details

See also
Status	Clinical Trial	Phase
Completed	`NCT01681004` - Investigation of Sacroiliac Fusion Treatment (INSITE)	N/A
Completed	`NCT02270203` - LOIS: Long-Term Follow-Up in INSITE/SIFI
Enrolling by invitation	`NCT05628142` - Tenon Medical CATAMARAN™ SI Joint Fusion System CT Scan Study	N/A
Active, not recruiting	`NCT04062630` - SI Joint Stabilization in Long Fusion to the Pelvis	N/A
Active, not recruiting	`NCT01640353` - Sacroiliac Joint Fusion With iFuse Implant System (SIFI)	Phase 4