Epilepsy, Healthy, Other, Tumor
Conditions
Brief summary
The purpose of the dMRI-1 data collection study is to establish a database of clinical images and limited medical history information from patients that have previously received a dMRI scan. All data collected will be de-identified. No safety or effectiveness assessments will be completed.
Interventions
DEVICEdMRI Scan
Data will be collected from cases where dMRI scans were obtained as part of the subject's previous treatment.
Sponsors
Medtronic Spinal and Biologics
Study design
Observational model
CASE_ONLY
Time perspective
RETROSPECTIVE
Eligibility
Sex/Gender
ALL
Healthy volunteers
Yes
Inclusion criteria
1. Patient is either ≥ 18 years and has previously received an acceptable dMRI scan(s) with at least 30 unique gradient directions or \< 18 years who has previously received an acceptable dMRI scan of any number of unique gradient directions and who is allowed to participate in this type of research project (e.g., IRB/EC approval with waiver of consent) per IRB/EC 2. Acceptable dMRI scan was completed prior to site activation in the study
Exclusion criteria
None
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Image assessment | Procedure |
Countries
Canada, United States
Outcome results
None listed