Fibricheck Detection cApabilities for Atrial Fibrillation

NCT06282380 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 330

Last updated 2024-06-27

No results posted yet for this study

Summary

Evaluation of accuracy of the FibriCheck Mobile Application on various smartphone devices, compared to the reference diagnosis.

Conditions

Interventions

DEVICE

FibriCheck Mobile Application

PPG measurement with reference diagnosis

Sponsors & Collaborators

  • Qompium NV

    lead INDUSTRY

Study Design

Allocation
NA
Purpose
OTHER
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
22 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-02-26
Primary Completion
2024-06-26
Completion
2024-06-26
FDA Device
Yes

Countries

  • United States
  • Belgium

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06282380 on ClinicalTrials.gov