Clinical Support on the iFuse Implant System® | SI-BONE

Clinical Evidence

Safety, Effectiveness, and Reliability

Clinical evidence is imperative and we recognize that product safety, effectiveness, and reliability are critical factors for providing exceptional patient care. 

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Clinical Studies

Clinical Articles

Clinical Studies of the iFuse Implant System.

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Clinical Evidence

Spotlight

iFuse Clinical Data

Unparalleled clinical evidence on the treatment of SI joint dysfunction with the iFuse Implant System®.

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Clinical Trials

To date we have sponsored multiple randomized controlled trials and several multi-center prospective trials .

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Publications

Review the medical literature on SI joint dysfunction, including burden of disease, prevalence, and diagnosis. 

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Research on Prevalence

of SI Joint Pain

  • 15-30% of individuals with lower back pain complaints actually had problems in their sacroiliac joint.1,2,3,4,5
  • 43% of post-lumbar fusion patients who were experiencing persistent or new onset lower back pain were shown to be symptomatic for SI joint disorders.14
Research on Prevalence of SI Joint Pain shows that 43% of post-lumbar fusion patients who were experiencing persistent or new onset lower back pain were shown to be symptomatic for SI joint disorders.

Rapid and Sustained Pain Relief: 

Rapid and Sustained Improvement 5 Year Outcomes from a Prospective Trail. At 12, 24 and 60 months, 82% of patients were satisfied and indicated that they would have the same surgery again for the same result.

iFuse: Backed By Evidence

The iFuse Implant System®, available since 2009, is the only device for treatment of SI joint dysfunction supported by significant published clinical evidence, including level 1 clinical data, showing safety, effectiveness and durability, including long lasting pain relief.

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Pelvis closeup with 3D Implants

4,000+Treating Physicians

110,000+iFuse Procedures Performed

140+iFuse Publications

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