LumiGuide Xperience registry version 2.0
Research type
Research Study
Full title
LumiGuide Xperience Registry
IRAS ID
329453
Contact name
Bijan Modarai
Contact email
Sponsor organisation
Philips Medical Systems Nederland B.V.
Duration of Study in the UK
2 years, 11 months, 30 days
Research summary
The main purpose of the LumiGuide Xperience Registry study is to determine the upgrades of the LumiGuide system product within the FORS technology.
The main function of the LumiGuide is that it visualizes the real-time 3D shape of endovascular devices in the context of the patient anatomy using Fiber Optic RealShape (FORS) technology during endovascular procedures of the peripheral, aortic and aortic side branch vasculature.
This study will collect patient data used within standard of care therapy during endovascular procedure using the FORS based image guidance related but not limited to: Radiation exposure, Procedure time. All Patients enrolled within duration of the study which will be up to 3 years will show for an endovascular procedure of the peripheral, arotic side branch vasculature.
The LumiGuide System is developed by Philips Medical Systems, a Philips Healthcare company. The proposed LumiGuide System is an approved device, CE and FDA certified. During the course of this study upgrades of the LumiGuide product within the FORS technology may be market released and become available.REC name
London - London Bridge Research Ethics Committee
REC reference
23/LO/0906
Date of REC Opinion
20 Feb 2024
REC opinion
Further Information Favourable Opinion