🏛️ Verified NIH Protocol • Sourced via U.S. National Library of Medicine (Last Synced: 2026-08-17)

The Ailliance Post-Market Clinical Study

🟢 Recruiting Protocol / Phase N/A ⚙️ Medical Device Protocol Sponsor: Medtronic Spinal and Biologics

🩺 Protocol Summary

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.

Primary Research Facility: University of Arizona (Tucson, Arizona)

📋 Basic Study Criteria & Logistics Checklist

0 of 3 Checked

Review these 3 basic logistical and protocol criteria extracted from the public NIH record. (This is a preliminary logistical checklist, not an official clinical eligibility determination).

Diagnosed with, undergoing evaluation for, or seeking treatment related to Spinal Deformity?

🔍 Study Population / Focus Area (Source: Protocol Primary Condition)

Aged 18 Years or older?

🔍 Protocol Specified Minimum Age: 18 Years

Able to attend required in-person clinic visits and study procedures at one of the participating study centers?

🔍 Logistical Requirement: 29 Registered Participating Sites

📍 Primary Site Map

Site: University of Arizona — Tucson, Arizona

📍 All Participating Trial Locations (29 Sites)

Multi-Center Trial

This protocol is enrolling participants across multiple clinical centers:

1. University of Arizona — Tucson, Arizona

2. OrthoArkansas — Little Rock, Arkansas

3. University of California Davis Medical Center — Sacramento, California

4. University of California, San Francisco (UCSF) — San Francisco, California

5. Indiana University School of Medicine — Bloomington, Indiana

6. Indiana Spine Group — Carmel, Indiana

7. The Orthopaedic Research Foundation (OrthoIndy) — Indianapolis, Indiana

8. Norton Leatherman Spine Specialists — Louisville, Kentucky

9. University of Maryland Medical Center — Baltimore, Maryland

10. Michigan Orthopaedic & Spine Surgeons — Rochester Hills, Michigan

11. University of Minnesota — Minneapolis, Minnesota

12. Washington University School of Medicine — St Louis, Missouri

13. Washington University School of Medicine — St Louis, Missouri

14. Rutgers University Department of Neurosurgery — New Brunswick, New Jersey

15. University at Buffalo — Buffalo, New York

16. University Hospitals Cleveland Medical Center — Cleveland, Ohio

17. The Ohio State University Wexner Medical Center — Columbus, Ohio

18. University of Pittsburgh Medical Center UPMC Presbyterian — Pittsburgh, Pennsylvania

19. Rhode Island Hospital University Orthopedic — Providence, Rhode Island

20. Tennessee Orthopaedic Alliance — Nashville, Tennessee

21. American Neurospine Institute, PLLC — Frisco, Texas

22. University of Virginia Health System — Charlottesville, Virginia

23. Virginia Spine Institute — Reston, Virginia

24. Centre Hospitalier Universitaire Dijon Bourgogne — Dijon, Bourgogne-Franche-Comté

25. Hôpital Roger Salengro — United States

📄 Print Doctor Discussion Sheet

Preview and print a 1-page summary with 5 tailored questions for your physician.

💰 Clinical Trial Costs & Insurance Coverage

Coverage for clinical trial participation varies depending on your health insurance policy, state legislation, and whether specific procedures are investigational research or routine medical care. Under federal law (Affordable Care Act § 2709), health insurers generally cannot drop coverage or refuse to pay for routine patient care costs incurred in approved clinical trials.

💡 Always ask the study coordinator for the trial's official Informed Consent Form, which outlines all sponsor-funded research items versus procedures billed to your insurance.

🏛️ Official Government Provenance

NIH ClinicalTrials.gov Protocol Record

NCT Identifier: NCT05856370 • Last Synced: 2026-08-17

View on ClinicalTrials.gov ↗