Clinical Outcome Measure at Stryker Spine

Recruiting now

Conditions studied: Degenerative Disc Disease, Degenerative Scoliosis

In brief

This is a multicenter, prospective, retrospective, Post Market Clinical Follow-up (PMCF) study in subjects who have undergone or will undergo surgery utilizing one or more Stryker devices according to Stryker cleared Instructions for Use (IFU).

Key facts

Study ID

NCT06226272

Run by

VB Spine, LLC

People needed

5222

Starts

2025-01-28

Expected to finish

2032-01-29

Last updated by the study team

2026-06-26

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• To be eligible to participate in the study, the potential subject must meet all inclusion criteria specific to the Stryker system being evaluated, please contact one of the participating investigators or see the device-specific cleared IFU, for further details.

You may not qualify if…

• The exclusion criteria are based on the contraindications as presented in the Stryker device cleared IFUs, please contact one of the participating investigators or see the device-specific cleared IFU, for further details.

Where it is running

• Mayo Clinic Florida — Jacksonville, Florida, United States (enrolling)
• MaineHealth Neurosurgery and Spine — Scarborough, Maine, United States (enrolling)
• Michigan Orthopaedic Surgeons — Southfield, Michigan, United States (enrolling)
• Cleveland Clinc — Cleveland, Ohio, United States (enrolling)
• Vanderbilt University Medical Center — Nashville, Tennessee, United States (enrolling)
• Texas Spine & Scoliosis — Austin, Texas, United States (enrolling)
• The University of Texas Health Science Center at Houston — Houston, Texas, United States (enrolling)

Full record on ClinicalTrials.gov

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