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Clinical Trial Summary

The purpose of the SAIF study is to evaluate the SImmetry Sacroiliac Joint Fusion System for fusion and pain reduction of the SI joint.


Clinical Trial Description

This is a prospective, non-randomized, single center study to collect data on fusion and pain reduction following implantation of the SImmetry device. Up to 15 total subjects will be implanted and followed for 24 months. Data will be collected pre-operatively, at implant, discharge, and at specified follow-up time points (6 weeks, 3 months, 6 months, 12 months, 24 months.) ;


Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


NCT number NCT02064322
Study type Observational
Source Zyga Technology, Inc.
Contact Lisa Ingham
Email lingham@zyga.com
Status Recruiting
Phase N/A
Start date February 2014
Completion date December 2016

See also
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