Status
Conditions
Treatments
About
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.
Enrollment
Sex
Ages
Volunteers
Inclusion criteria
Exclusion criteria
Primary purpose
Allocation
Interventional model
Masking
1,000 participants in 3 patient groups
Loading...
Central trial contact
Nuria Mahmood; Katelynn Hamer
Data sourced from clinicaltrials.gov
Clinical trials
Research sites
Resources
Legal