Stryker Spinal Devices for Degenerative Disc Disease and Scoliosis
This study is looking at how well different Stryker spinal devices work and how safe they are for people with degenerative disc disease or degenerative scoliosis. These devices are used in spinal fusion (a surgery to join two or more bones in your spine) or spinal deformities correction. The study will follow people who have already had or will have surgery using these devices. Researchers will collect information for up to 24 months after surgery to understand the long-term performance and safety of these devices. You may be able to join if you are 18 years or older and meet specific criteria for the Stryker device being evaluated. The study is currently unclear on its recruitment status.
- Study design
- This is an observational study, meaning researchers will collect information without giving new treatments. It plans to include up to 5222 participants.
- What's involved
- Not specified in the trial record.
- Compensation
- Not stated in the trial record.
- Follow-up
- Participants will be followed for up to 24 months after their surgery.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
Clinical Outcome Measure at Stryker Spine
At a glance
Conditions
Where it's being run
7 sites across 6 statesStudy leadership
- Jad G. Khalil, MD · PRINCIPAL_INVESTIGATOR · Michigan Orthopaedic Surgeons
Who to contact
Opens a ready-to-send draft in your own email app — review before sending.
What this trial measures
- S-S-102-ABaseline through 24-months post-op.
Mean change in the subject's Neck Disability Index (NDI) score.
- S-S-102-BBaseline through 24-months post-op.
Mean change in the subject's Oswestry Disability Index (ODI) score.
- S-S-102-CBaseline through 24-months post-op.
Mean change in the subject's Scoliosis Research Society-22 revised (SRS-22r).