Status: Recruiting
The Ailliance Post-Market Clinical Study
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.
Participants needed: 1,000
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Medtronic Spinal and BiologicsUpdated: Jun 30, 2026Locations: 28
Eligibility criteria
Subject provides written informed consent per institution and/or geographical re... [+3]
Subject is currently enrolled or plans to enroll in concurrent drug/device/biolo... [+3]