LOIS ICD
Research type
Research Study
Full title
Clinical Evaluation of the LOIS Smartband in patients undergoing elective Subcutaneous ICD implantation.
IRAS ID
264962
Contact name
Phang Boon Lim
Contact email
Sponsor organisation
LOIS Medical ltd
Duration of Study in the UK
0 years, 6 months, 1 days
Research summary
Non-invasive, pain-free clinical evaluation of a wearable/proximity sensor designed to detect a high voltage therapeutic shock received by a patient from their Implantable Cardioverter Defibrillator (ICD) during defibrillation threshold testing (DFT), which is a routine part of the clinical procedure.
The principle purpose of the evaluation is to determine that the LOIS ICD Smartband does in fact detect an ICD discharge. The LOIS Smartband has been bench tested with excellent outcomes but has not been tested whilst being worn by a patient.
REC name
London - Fulham Research Ethics Committee
REC reference
19/LO/1970
Date of REC Opinion
16 Jan 2020
REC opinion
Unfavourable Opinion