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Treatment of Sacroiliac Dysfunction With SI-LOK® Sacroiliac Joint Fixation SI-SI-LOK

NCT01861899 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 46

Last updated 2020-09-11

No results posted yet for this study

Summary

The objective of this study is to gather clinical data on SI-LOK® for the treatment of sacroiliac joint dysfunction.

The purpose of this prospective study is to evaluate clinical and radiographic outcomes, intra-operative parameters, patient satisfaction and work status following a procedure using SI-LOK® for treatment of sacroiliac joint dysfunction with a minimum of three screws.

Conditions

  • Joint Dysfunction

Interventions

DEVICE

SI-LOK

Sacro-iliac joint fusion

Sponsors & Collaborators

  • Globus Medical Inc

    lead INDUSTRY

Principal Investigators

  • Michael Barnum, MD · Northwestern Medical Center, St Albans, VT 05478

Eligibility

Min Age
21 Years
Max Age
70 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-05-02
Primary Completion
2018-07-05
Completion
2019-04-11

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 NCT01861899 on ClinicalTrials.gov