Comparison of ocular- and monitor-based interventions
Phase 4
- Conditions
- supratentorial non-eloquent brain tumors
- Registration Number
- DRKS00016674
- Lead Sponsor
- Charité Campus Charité Mitte
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 20
Inclusion Criteria
circumscribed supratentorial lesion in non-eloquent location, age > 18 years, eligibility for both modalities, operating surgeon trained in both modalities
Exclusion Criteria
multimorbidity
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The study investigates the impact of the new operating mode (monitor-based) on intraoperative workflows in comparison with the established standard (surgical microscope wirth oculars).
- Secondary Outcome Measures
Name Time Method The study further investigates the surgeons' satisfaction with the new device (exoscope) in comparison with the established standard (surgical microscope wirth oculars) using validated questionnaires (System Usability Scale, Surgical Task Load Index) and short user interviews.