The Ailliance Post-Market Clinical Study (NCT05856370)
The Ailliance Post-Market Clinical Study: All enablIng technoLogies, bioLogics, IDS, And Core spiNe produCt collEction
🩺 Plain-English Summary (8th-Grade Level)
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.
Who can join: Review the eligibility criteria below.
Location: University of Arizona — Tucson, Arizona
Age range: 18 Years
🧪 Interventions in This Study
📋 "Do I Qualify?" — 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria ↗
📍 All Participating Trial Locations (29 Sites)
Showing the first 25 of 29 sites.
- University of Arizona — Tucson, Arizona
- OrthoArkansas — Little Rock, Arkansas
- University of California Davis Medical Center — Sacramento, California
- University of California, San Francisco (UCSF) — San Francisco, California
- Indiana University School of Medicine — Bloomington, Indiana
- Indiana Spine Group — Carmel, Indiana
- The Orthopaedic Research Foundation (OrthoIndy) — Indianapolis, Indiana
- Norton Leatherman Spine Specialists — Louisville, Kentucky
- University of Maryland Medical Center — Baltimore, Maryland
- Michigan Orthopaedic & Spine Surgeons — Rochester Hills, Michigan
- University of Minnesota — Minneapolis, Minnesota
- Washington University School of Medicine — St Louis, Missouri
- Washington University School of Medicine — St Louis, Missouri
- Rutgers University Department of Neurosurgery — New Brunswick, New Jersey
- University at Buffalo — Buffalo, New York
- University Hospitals Cleveland Medical Center — Cleveland, Ohio
- The Ohio State University Wexner Medical Center — Columbus, Ohio
- University of Pittsburgh Medical Center UPMC Presbyterian — Pittsburgh, Pennsylvania
- Rhode Island Hospital University Orthopedic — Providence, Rhode Island
- Tennessee Orthopaedic Alliance — Nashville, Tennessee
- American Neurospine Institute, PLLC — Frisco, Texas
- University of Virginia Health System — Charlottesville, Virginia
- Virginia Spine Institute — Reston, Virginia
- Centre Hospitalier Universitaire Dijon Bourgogne — Dijon, Bourgogne-Franche-Comté
- Hôpital Roger Salengro — Lille,
📞 Contact the Study Coordinator
Phone: (763) 526-8124
Email: lauren.k.oien@medtronic.com
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
💰 Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
More studies in Spinal Deformity
- Analysis of Pedicle Screw Accuracy to Plan Using Medtronic Mazor Robotic System — Columbus, Ohio
- Prospective, Multi-Center Adult Spinal Deformity Outcomes Database Registry — La Jolla, California
- Intraoperative Alignment in Adult Spinal Deformity Surgery — New York, New York
- Tranexamic Acid in Adult Spinal Deformity Surgery — New York, New York
Explore by condition: All Spinal Deformity clinical trials
💡 How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.