CT Follow-Up of the SImmetry Sacroiliac Joint Fusion System

Zyga Technology, Inc.19 enrolled

Overview

This study will evaluate long-term follow-up of subjects implanted with the SImmetry Sacroiliac (SI) Joint Fusion System (SImmetry).

Study Type

OBSERVATIONAL

Enrollment

Conditions

Sacroiliitis

Interventions

SImmetry Sacroiliac Joint Fusion SystemDEVICE

Minimally invasive surgery for implantation of the SImmetry System

Eligibility

Sex: ALL

Medical Language ↔ Plain English

Inclusion Criteria: * Patient must have a SImmetry device implanted. * Patient is willing to comply with study procedures and provide informed consent. Exclusion Criteria: * Patient is physically unable to return to the clinic for CT imaging.

Outcomes

Primary Outcomes

SI Joint Fusion (CT evidence of SI joint fusion)

CT evidence of SI joint fusion evaluated by a core laboratory

Time frame: 12 months

Secondary Outcomes

SI Joint Pain (CT evidence of SI joint fusion)

evaluated by a core laboratory

Time frame: 24 months

Data from ClinicalTrials.gov

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