MACENDOR: Magnetocardiography Endocrine Registry

Sponsor
Genetesis Inc. (Industry)
Overall Status
Recruiting
CT.gov ID
NCT04739254
Collaborator
(none)
250
1
23.6
10.6

Study Details

Study Description

Brief Summary

Endocrine disorders like Type 2 diabetes mellitus (T2DM) represent complex cardiometabolic disease processes affecting approximately 462 million individuals worldwide and is associated with a two- to three-fold increase in cardiovascular mortality. Individuals with T2DM are at an increased risk of developing cardiovascular disease. Research has shown individuals with T2DM and no previous history of coronary artery disease are still at similar risk rates for cardiovascular events as patients with a prior myocardial infarction. The MAgenetoCardiography ENDOcrine Registry (MACENDOR) study is designed to collect CardioFlux scans on a select group of volunteers who are high-risk patients with endocrine disorders. CardioFlux is used as a noninvasive magnetocardiography (MCG) tool that analyzes and records the magnetic fields of the heart to screen volunteers for heart disease. There will be a 12-month duration of the study where we propose to collect screening data from approximately 250 volunteers who present to the Genetesis facility for a 5-minute CardioFlux scan. The volunteers will be contacted at intervals over a 1-year period for follow-up data and may choose whether or not they would like to provide follow-up data or participate in another scan.

Condition or Disease Intervention/Treatment Phase
  • Other: Not an intervention

Study Design

Study Type:
Observational
Anticipated Enrollment :
250 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Magnetocardiography Endocrine Registry
Actual Study Start Date :
Dec 14, 2020
Anticipated Primary Completion Date :
Dec 1, 2022
Anticipated Study Completion Date :
Dec 1, 2022

Outcome Measures

Primary Outcome Measures

  1. Accuracy statistics [12 months]

    analyzing the accuracy of CardioFlux

  2. Specificity statistics [12 months]

    analyzing the specificity of CardiFlux

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. ≥ 18 years of age at the time of enrollment

  2. Patients deemed at risk for cardiovascular disease from endocrine disorders

Exclusion Criteria:
  1. < 18 years of age

  2. Patients unable to fit into device

  3. Non-ambulatory patients

  4. Positive response(s) on CardioFlux Pre-Screening Form

  5. Patients with claustrophobia or unable to lie supine for five minutes

  6. Pregnant women

  7. Poor candidates for follow-up (e.g., no access to phone)

  8. Prisoners

Contacts and Locations

Locations

Site City State Country Postal Code
1 Genetesis Facility Mason Ohio United States 45040

Sponsors and Collaborators

  • Genetesis Inc.

Investigators

  • Principal Investigator: Anthony Senagore, M.D., Genetesis Inc.

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Genetesis Inc.
ClinicalTrials.gov Identifier:
NCT04739254
Other Study ID Numbers:
  • 1000-4
First Posted:
Feb 4, 2021
Last Update Posted:
Jan 21, 2022
Last Verified:
Jan 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:
Yes
Product Manufactured in and Exported from the U.S.:
No
Keywords provided by Genetesis Inc.
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jan 21, 2022