Lumbar & Sacroiliac Fusion Study Involving Previously Implanted Devices

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorSpinal Simplicity LLC

About this trial

This study is a multi-center, observational, prospective and retrospective data collection study

Eligibility criteria

Qualifiers

Be 18 years of age or older at the time of enrollment

Be willing and able to provide informed consent and comply with study visit requirements

Subjects who received a Spinal Simplicity fusion implant(s) (Minuteman G5, Liberty, and/or Patriot) between April 1, 2022 and March 31, 2025

Disqualifiers

Unable to provide consent and complete prospective data collection

Women who are pregnant, or may become pregnant, during the course of the study

Contraindication to CT scanning, in the opinion of the investigator

Trial design

Treatments tested in this trial

  • Cat Scan, if applicable

Treatment groups

500 Participants
are divided into 1 treatment group

Sponsors and collaborators