LithoVue Elite (LVE) Registry
Status: Withdrawn
Intervention Type: Device
Study Type: Observational
SUMMARY
To obtain postmarket safety and efficacy data on Boston Scientific LithoVue™ Elite System.
Eligibility
Participation Requirements
Sex: All
Healthy Volunteers: f
View:
• Subject intends to undergo diagnostic and/or therapeutic procedure in the urinary tract with Boston Scientific LithoVue Elite System
• Subject is able to accurately detect and report pain
• Subject is willing and able to complete subject questionnaire at specified time points
• Subject is willing and able to return for all follow-up visits
Time Frame
Start Date: 2023-04-01
Completion Date: 2023-12-01
Treatments
Pressure Monitoring
Subjects in this cohort will undergo ureteroscopic procedure using LithoVue Elite pressure monitoring single use flexible scope, real-time pressure monitoring technology, which will provide surgeons with intraluminal pressure data in the kidneys and ureter.
Non-Pressure Monitoring
Subjects in this cohort will undergo ureteroscopic procedure using LithoVue Elite Non-pressure monitoring single use flexible scope.
Related Therapeutic Areas
Sponsors
Leads: Boston Scientific Corporation