CARDIOSECUR: CardioSecur Connected Electrocardiography in General Care

Sponsor
Lille Catholic University (Other)
Overall Status
Completed
CT.gov ID
NCT03351660
Collaborator
(none)
338
9
27.4
37.6
1.4

Study Details

Study Description

Brief Summary

Heart disease symptoms are a frequent reason of consultation in general medical practice. Only a few general practitioners are equipped with a 12 lead Electrocardiography (ECG) whereas this test is extremely useful for diagnosis orientation in cases of cardiac diseases.Cardiosecur allows the realization of a 15 or 22 leads ECG with only 4 electrodes connected to a smartphone or a tablet with an automatic interpretation function. The goal of the study is to evaluate the diagnostic value of Cardiosecur device regarding cardiac symptoms in family practice.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: connected ECG

Detailed Description

This study will be a multicenter, single arm, non randomized trial testing the incremental diagnosis value of Cardiosecur ECG regarding cardiac disease in general care.

Ten general practitioners will be given a Cardiosecure ACTIVE device with a tablet and perform an EKG to their consecutive patients who meet the inclusion criteria.

Inclusion criteria

  • Recent cardiovascular symptom < 7 days (chest pain, dyspnea, palpitation, heart failure or transient loss of consciousness) or physical examination leading in possible cardiac cause.

  • Aged over 18 years

  • signed the informed consent

  • A questionnaire regarding the diagnosis orientation based on the patients' symptoms and physical examination will be given to GPs before and after the ECG realization and automatic interpretation to evaluate whether the ECG modified the diagnosis.

If the GP need further exploration to conclude or if the patient is oriented to an hospital or a specialist, the reference diagnosis will be defined at the end of these explorations. Otherwise, the diagnostic will be defined at the end of the GP consultation.

  • A questionnaire regarding the ease of use of the Cardiosecure device will be filled by the patients.

  • Time for ECG realization will be recorded.

  • All the ECG and their automatic interpretation will be stored anonymously according to bioethics laws and then reviewed by 2 experienced cardiologists blinded to the results of the automatic interpretation. The interobserver reproducibility as well as the comparison with the Cardiosecur automatic interpretation will be analyzed.

Study Design

Study Type:
Observational
Actual Enrollment :
338 participants
Observational Model:
Case-Only
Time Perspective:
Cross-Sectional
Official Title:
Diagnostic Value of the CardioSecur Connected EcG in General Care: The Connected EGG-study.
Actual Study Start Date :
Dec 15, 2016
Actual Primary Completion Date :
Mar 28, 2019
Actual Study Completion Date :
Mar 28, 2019

Outcome Measures

Primary Outcome Measures

  1. Performance of ECG Cardiosecur [Baseline]

    Proportion of correct diagnosis before and after Cardiosecur

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Recent cardiovascular symptoms < 7 days (chest pain, dyspnea, palpitations, heart failure or transient loss of consciousness) or physical examination suggesting cardiac disease.

  • Patients aged over 18 years

  • Signed the informed consent

Exclusion Criteria:

Contacts and Locations

Locations

Site City State Country Postal Code
1 Aire-sur-la-Lys France 62120
2 Chenôve France 21300
3 Cysoing France 59830
4 Dijon France 21600
5 Iteuil France 86240
6 Montreuil-sur-mer France 62170
7 Poitiers France 86440
8 Roubaix France 59100
9 Vervins France 02140

Sponsors and Collaborators

  • Lille Catholic University

Investigators

  • Principal Investigator: Aymeric Menet, MD, Groupement des Hôpitaux de l'Institut Catholique de Lille

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Lille Catholic University
ClinicalTrials.gov Identifier:
NCT03351660
Other Study ID Numbers:
  • RCP-0063
First Posted:
Nov 24, 2017
Last Update Posted:
Apr 12, 2022
Last Verified:
Apr 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Apr 12, 2022