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Clinical Outcome and Fusion Results Using the SiJoin® Transfixing Sacroiliac Fusion Device

NCT05712850 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 25

Last updated 2023-07-24

No results posted yet for this study

Summary

The purpose of this clinical study is to evaluate fusion of the SI joint(s) and any reduction in VAS pain scores in a prospective cohort of patients utilizing the SiJoin® Transfixing Sacroiliac Fusion Device in patients that received sacroiliac fusion, without ancillary stabilization devices.

Conditions

  • Sacroiliitis
  • Sacroiliac Joint Dysfunction
  • Iatrogenic Injury
  • Osteitis Condensans Ilii
  • Pelvic Fracture

Interventions

PROCEDURE

SiJoin® Transfixing Sacroiliac Fusion Device

Sacroiliac Fusion

Sponsors & Collaborators

  • VG Innovations, LLC

    lead INDUSTRY

Eligibility

Min Age
18 Years
Max Age
85 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2023-01-19
Primary Completion
2024-01-18
Completion
2025-03-31

Countries

  • United States

Study Locations

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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 NCT05712850 on ClinicalTrials.gov