Condition: Spinal Deformity · Spinal Degenerative Disorder · Spinal Fusion Failure · Sponsor: Medtronic Spinal and Biologics
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.
This description comes directly from the study's public registry record.
Lauren Oien · +17635268124 · lauren.k.oien@medtronic.com
Erwan Diarra · +33 7 86 55 72 84 · erwan.diarra@medtronic.com
Always discuss trial participation with your own doctor first.
| University of Arizona | Tucson, Arizona, United States | Recruiting |
| OrthoArkansas | Little Rock, Arkansas, United States | Recruiting |
| University of California Davis Medical Center | Sacramento, California, United States | Recruiting |
| University of California, San Francisco (UCSF) | San Francisco, California, United States | Recruiting |
| Indiana University School of Medicine | Bloomington, Indiana, United States | Recruiting |
| Indiana Spine Group | Carmel, Indiana, United States | Recruiting |
| The Orthopaedic Research Foundation (OrthoIndy) | Indianapolis, Indiana, United States | Recruiting |
| Norton Leatherman Spine Specialists | Louisville, Kentucky, United States | Recruiting |
| University of Maryland Medical Center | Baltimore, Maryland, United States | Recruiting |
| Michigan Orthopaedic & Spine Surgeons | Rochester Hills, Michigan, United States | Recruiting |
| University of Minnesota | Minneapolis, Minnesota, United States | Recruiting |
| Washington University School of Medicine | St Louis, Missouri, United States | Recruiting |
+ 16 more locations — full list on the registry record.
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Source record: clinicaltrials.gov/study/NCT05856370