RecruitingNot ApplicableNCT07204288

Lumbar & Sacroiliac Fusion Study Involving Previously Implanted Devices

Lumbar & Sacroiliac Fusion Study: Multi-Center Prospective Radiographic Study on Subjects Previously Implanted With Spinal Simplicity Lumbar and/or Sacroiliac Fusion Device(s)


Sponsor

Spinal Simplicity LLC

Enrollment

500 participants

Start Date

Sep 11, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

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


Eligibility

Min Age: 18 Years

Inclusion Criteria3

  • 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

Exclusion Criteria3

  • 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

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Interventions

OTHERCat Scan, if applicable

CT imaging is being used to assess fusion in participants with previously implanted devices that were not explanted.


Locations(3)

Crimson Pain Management

Overland Park, Kansas, United States

Nuroscience Research Center

Overland Park, Kansas, United States

Nura Precision Pain Management

Edina, Minnesota, United States

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NCT07204288


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