Spots Global Cancer Trial Database for The Ailliance Post-Market Clinical Study
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Trial Identification
Brief Title: The Ailliance Post-Market Clinical Study
Official Title: The Ailliance Post-Market Clinical Study: All enablIng technoLogies, bioLogics, IDS, And Core spiNe produCt collEction
Study ID: NCT05856370
Study Description
Brief 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 for up to 24 months. The Ailliance clinical study is intended to collect data congruous with routine clinical care practices.
Detailed Description:
Keywords
Eligibility
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
Locations
University of California, San Francisco (UCSF), San Francisco, California, United States
Indiana University School of Medicine, Bloomington, Indiana, United States
Indiana Spine Group, Carmel, Indiana, United States
The Orthopaedic Research Foundation (OrthoIndy), Indianapolis, Indiana, United States
Norton Leatherman Spine Specialists, Louisville, Kentucky, United States
Michigan Orthopaedic & Spine Surgeons, Rochester Hills, Michigan, United States
University of Minnesota, Minneapolis, Minnesota, United States
The Ohio State University Wexner Medical Center, Columbus, Ohio, United States
Rhode Island Hospital University Orthopedic, Providence, Rhode Island, United States
Tennessee Orthopaedic Alliance, Nashville, Tennessee, United States
American Neurospine Institute, PLLC, Frisco, Texas, United States
Contact Details
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