Epilepsy, Other, Tumor
Conditions
Brief summary
The purpose of the VIVID-1 data collection study is to establish a database of clinical images and associated technical files from commercial cases using the Visualase Thermal Therapy System (VTTS). All data collected will be de-identified. No safety or effectiveness assessments will be completed.
Interventions
Patients who have previously received treatment with VTTS when used as intended.
Sponsors
MedtronicNeuro
Study design
Observational model
CASE_ONLY
Time perspective
RETROSPECTIVE
Eligibility
Sex/Gender
ALL
Healthy volunteers
No
Inclusion criteria
1\. Patient correlating with the de-identified data set to be collected received standard of care treatment using the Visualase System prior to the date of site activation.
Exclusion criteria
1. Patient correlating with the de-identified data set to be collected is a minor (less than 18 years old, or as defined by local policy) that is not allowed to participate in this type of research project (eg, IRB approval with waiver of consent) per IRB policy 2. Patient correlating with the de-identified data set to be collected is enrolled in the Medtronic SLATE trial
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Image assessment | During the Procedure | Identify pathologies and tissue types prescribed Visualse Thermal Therapy |
Countries
United States
Outcome results
None listed