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SAIF: Sacroiliac Fusion Study

NCT02064322 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 2

Last updated 2016-03-31

No results posted yet for this study

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.

Conditions

  • Sacroiliac Joint Dysfunction

Interventions

DEVICE

SImmetry Implant

The SImmetry system is commercially available. The implanted devices consist of a range of thread-tapping cannulated implants designed to transfix the sacrum and ilim, providing stability for intra-articular fusion. The SImmetry Surgical Instruments include standard manual surgical instruments used to access and prepare the sacroiliac joint space for intra-articular fusion.

Sponsors & Collaborators

  • Zyga Technology, Inc.

    lead INDUSTRY

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-02-28
Primary Completion
2016-03-31
Completion
2016-03-31

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02064322 on ClinicalTrials.gov