The Ailliance Post-Market Clinical Study: All enablIng technoLogies, bioLogics, IDS, And Core spiNe produCt collEction
Status: Recruiting
Location: See all (23) locations...
Intervention Type: Device
Study Type: Interventional
Study Phase: Not Applicable
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.
Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:
• Subject provides written informed consent per institution and/or geographical requirements.
• 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 cranial and/or spinal indication(s).
• Subject is at least 18 years of age or minimum legal age as required by local regulations.
• Subject agrees to complete all required assessments per the Schedule of Events.
Locations
United States
Arkansas
OrthoArkansas
RECRUITING
Little Rock
Arizona
University of Arizona
RECRUITING
Tucson
California
University of California Davis Medical Center
RECRUITING
Sacramento
University of California, San Francisco (UCSF)
RECRUITING
San Francisco
Indiana
Indiana University School of Medicine
RECRUITING
Bloomington
Indiana Spine Group
RECRUITING
Carmel
The Orthopaedic Research Foundation (OrthoIndy)
RECRUITING
Indianapolis
Kentucky
Norton Leatherman Spine Specialists
RECRUITING
Louisville
Maryland
University of Maryland Medical Center
RECRUITING
Baltimore
Michigan
Michigan Orthopaedic & Spine Surgeons
RECRUITING
Rochester Hills
Minnesota
University of Minnesota
RECRUITING
Minneapolis
Missouri
Washington University School of Medicine
RECRUITING
St Louis
Washington University School of Medicine
RECRUITING
St Louis
New York
University at Buffalo
RECRUITING
Buffalo
Ohio
The Ohio State University Wexner Medical Center
RECRUITING
Columbus
Pennsylvania
University of Pittsburgh Medical Center UPMC Presbyterian
RECRUITING
Pittsburgh
Rhode Island
Rhode Island Hospital University Orthopedic
RECRUITING
Providence
Tennessee
Tennessee Orthopaedic Alliance
RECRUITING
Nashville
Texas
American Neurospine Institute, PLLC
RECRUITING
Frisco
Virginia
University of Virginia Health System
RECRUITING
Charlottesville
Virginia Spine Institute
RECRUITING
Reston
Other Locations
France
Hôpital Roger Salengro
RECRUITING
Lille
Spain
Hospital Vall D'Hebron
RECRUITING
Barcelona
Contact Information
Primary
Katelynn Hamer
katelynn.m.hamer@medtronic.com
630-544-9247
Backup
Nuria Mahmood
nuria.mahmood@medtronic.com
763-505-4024
Time Frame
Start Date:2023-05-01
Estimated Completion Date:2031-05
Participants
Target number of participants:1000
Treatments
Other: Receiving eligible Medtronic device(s) from all product groups
Powered Systems, Instruments, and Imaging device(s), Advanced Energy device(s), Robotics and Navigation, Rods and Screws, Interbodies and Biologics, Spinal Tethers, and Other Spinal Hardware device(s)