CT Follow-Up of the SImmetry Sacroiliac Joint Fusion System

Status

Completed

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT02425631

Enrollment

Registered

2015-04-24

Start date

2014-10-31

Completion date

2016-06-30

Last updated

2016-09-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Sacroiliitis

Keywords

SI joint fusion, SI joint pain, SI joint, SI joint treatment, SI joint disease, Sacroiliac joint, Simmetry

Brief summary

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

Interventions

DEVICESImmetry Sacroiliac Joint Fusion System

Minimally invasive surgery for implantation of the SImmetry System

Study design

Observational model

COHORT

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Healthy volunteers

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.

Design outcomes

Primary

Measure	Time frame	Description
SI Joint Fusion (CT evidence of SI joint fusion)	12 months	CT evidence of SI joint fusion evaluated by a core laboratory

Secondary

Measure	Time frame	Description
SI Joint Pain (CT evidence of SI joint fusion)	24 months	evaluated by a core laboratory

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026