The Ailliance Post-Market Clinical Study
Recruiting
N/A
Interventional Study
Spinal Deformity
Spinal Degenerative Disorder
Spinal Fusion Failure
Spinal Trauma
Spinal Tumor Case
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 and older
- Sex
- Any
- Study type
- Interventional
- Purpose
- Health Services Research
- Participants needed
- 1,000 (estimated)
- Sponsor
- Medtronic Spinal and Biologics · Industry
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About This Trial
The purpose of this clinical study is to collect performance and safety data for post-market Medtronic devices indicated for cranial and/or spinal indication(s). Subjects are enrolled and followed postoperatively to 24 months. The Ailliance clinical study is intended to collect data congruous with routine clinical care practices.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
1. Subject provides written informed consent per institution and/or geographical requirements.
2. Subject is intended to receive or be treated with an eligible Medtronic Cranial and Spinal Technology (CST) device(s) (see product appendices), used alone or in combination, for a c…
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