Sacroiliac Joint Fusion With iFuse Implant System (SIFI) — SIFI

Sacroiliac Joint Disruption Clinical Trial

Official title:
Sacroiliac Joint Fusion With iFuse Implant System (SIFI)

Status Active, not recruiting

Clinical Trial Summary

The purpose of this study is to evaluate the use of the iFuse Implant System to treat degenerative sacroiliitis (arthritis of the SI joint) and sacroiliac disruption (abnormal separation or tearing of the sacroiliac joint). The iFuse Implant System (iFuse device) is a medical device that is surgically implanted into the sacroiliac (SI) joint during a minimally invasive surgical procedure (one that uses a smaller incision and less damage to the skin and other tissues than standard surgery). The purpose of implanting the device is to stabilize and fuse the SI joint.

Clinical Trial Description

n/a

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT01640353
Study type	Observational
Source	SI-BONE, Inc.
Contact
Status	Active, not recruiting
Phase	Phase 4
Start date	July 2012
Completion date	December 2015

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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
Recruiting	`NCT05633888` - Post-Market Feasibility Study of the Tenon Medical CATAMARAN™ SI Joint Fusion System	N/A
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