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Study identifier: NCT06355791 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Post-Market Clinical Study of Functional Motion Outcomes in Subjects Treated With the Minuteman Device

Condition: Degenerative Conditions of the Lumbar Spine · Lumbar Spinal Stenosis · Spondylolisthesis  ·  Sponsor: Spinal Simplicity LLC

PhaseNA
Planned participants150
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

This is a prospective, multi-center open-label single arm post-market study where the purpose is to evaluate the effectiveness and safety of the market approved Spinal Simplicity Minuteman G5 MIS Fusion Plate and bone graft material in patients with degenerative conditions of the lumbar spine resulting in chronic low back pain with lower extremity symptoms and concurrent neurogenic claudication. The indication for the device under study is degenerative conditions of the lumbar spine resulting in back pain with lower extremity symptoms and neurogenic claudication.

This description comes directly from the study's public registry record.

Talk to the study team

Echo Cundiff  ·  913-451-4414  ·  ecundiff@spinalsimplicity.com

Adam Rogers  ·  913-451-4414  ·  arogers@spinalsimplicity.com

Always discuss trial participation with your own doctor first.

Locations (6)

Vista Clinical ResearchNewnan, Georgia, United StatesRecruiting
Comprehensive Pain & Spine SpecialistsIndianapolis, Indiana, United StatesRecruiting
University of Kansas Medical CenterKansas City, Kansas, United StatesNot Yet Recruiting
Nura Precision Pain ManagementEdina, Minnesota, United StatesRecruiting
Pacific Sports & SpineEugene, Oregon, United StatesRecruiting
Spine & Nerve Center of the VirginiasCharleston, West Virginia, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT06355791