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NCT01861899

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

Completed Last updated 11 September 2020
What this trial tests

trial testing SI-LOK in Joint Dysfunction in 46 participants. Completed in 11 April 2019.

Timeline
2 May 2013
Primary endpoint
5 July 2018
11 April 2019

Quick facts

Lead sponsorGlobus Medical Inc
StatusCompleted
Study typeOBSERVATIONAL
Enrollment46
Start date2 May 2013
Primary completion5 July 2018
Estimated completion11 April 2019
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Globus Medical Inc — full company profile →

Who can join

Adults 21 to 70, any sex, with Joint Dysfunction. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other Globus Medical Inc trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT01861899.

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