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Search / Trial NCT03636230

Remote Patient Management of CIEDs - Brady Devices

Launched by RATIKA PARKASH · Aug 15, 2018

Trial Information

Current as of June 26, 2025

Recruiting

Keywords

ClinConnect Summary

This clinical trial is exploring the use of remote monitoring for patients with pacemakers. Remote monitoring allows doctors to check your pacemaker's performance and your heart health from a distance, without needing you to come into the clinic every time. Although this technology is commonly used around the world, in Canada, it has mostly been used for a different type of heart device called an implantable defibrillator. This study aims to see how effective and safe it is to use remote monitoring just for pacemaker patients, while still allowing for in-person visits when necessary.

To join the study, you need to be between 65 and 74 years old, have a Medtronic or Abbott pacemaker that can be monitored remotely, and have access to a smartphone or tablet. You should also be able to give your consent to participate. Participants will use a patient-friendly electronic platform to keep track of their health and will have the opportunity for regular check-ins with their healthcare team. This study hopes to show that remote monitoring can be a better, more cost-effective way to manage pacemaker care while ensuring that patients receive timely support.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Patients with a Medtronic or Abbott pacemaker capable of remote monitoring.
  • Able to provide consent.
  • Age \>/= 18 years
  • Exclusion Criteria:
  • No access to a family physician or general practioner
  • Participation in the RPM CIED pilot study
  • Unreliable automated capture verification function by the device in pacemaker-dependent patients

About Ratika Parkash

Ratika Parkash is a dedicated clinical trial sponsor focused on advancing medical research and improving patient outcomes through innovative therapeutic solutions. Committed to rigorous scientific standards and ethical practices, the organization collaborates with leading healthcare professionals and research institutions to design and implement clinical trials across various therapeutic areas. With a strong emphasis on patient safety and data integrity, Ratika Parkash aims to contribute valuable insights to the medical community, ultimately enhancing treatment options and quality of care for patients worldwide.

Locations

Newmarket, Ontario, Canada

Halifax, Nova Scotia, Canada

Montréal, Quebec, Canada

Kitchener, Ontario, Canada

Saint John's, Newfoundland And Labrador, Canada

Montréal, Quebec, Canada

Quebec City, Quebec, Canada

Calgary, Alberta, Canada

Victoria, British Columbia, Canada

London, Ontario, Canada

Sherbrooke, Quebec, Canada

Patients applied

0 patients applied

Trial Officials

Ratika Parkash, MD FRCPC

Principal Investigator

Nova Scotia Health Authority

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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