iBeat Wristwatch Validation Study

Arrythmia, Cardiac Clinical Trial

Official title: Validation of Signal Waveforms in a Consumer-based Wristwatch Prototype Device During Standard Cardiac Procedures

Status Completed

Clinical Trial Summary

The iBeat Study is a single-center, prospective, unblinded validation of the photoplethysmography (PPG) and tissue oximetry (TO) signal waveforms recorded from a wrist-based sensor devices.

Clinical Trial Description

The goal of the proposed research is to validate PPG and TO signal waveforms recorded from a wist-based sensor device, which is worn on one or both arms, during catheter ablation, device interrogation, and defibrillation threshold testing (DFT). It is a non-invasive procedure that will include placing a wrist-based sensor on subjects who consent participate. Data collected from routine clinical care devices used during these procedures (catheter ablations, device interrogations, and DFTs) will confirm data collected from the iBeat wristwatch. ;

Related Conditions & MeSH terms

• Arrhythmias, Cardiac
• Arrythmia, Cardiac

• NCT number: NCT03711695
• Study type: Observational
• Source: University of California, San Francisco
• Status: Completed
• Start date: March 22, 2018
• Completion date: December 30, 2018