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OpenTrials
Completed

NCT Number: NCT03317964

Genetic Basis of Pacing-induced Cardiomyopathy

The purpose of this study is to collect a saliva sample from patients with a pacemaker to study genes involved in cardiomyopathy, a condition where the heart muscle is abnormal.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Robert Packer Hospital

Sayre, Pennsylvania, 18840, United States

About this study

DNA will be extracted from the saliva to test for changes in genes related to cardiomyopathy.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients who have been assessed for cardiomyopathy

Exclusion criteria

  • Patients who do not have adequate follow up care to determine if they do or do not have cardiomyopathy

Treatment and study plan

Saliva Sample

Other

Extract sample of saliva only once

Primary outcomes

  1. Number of participants with genotype frequency

    Time frame: through study completion, an average of 1 year

    Number of participants with genotype frequency based on genetic testing of saliva samples

Sponsors and collaborators

Lead sponsor

The Guthrie Clinic

Other

Registry information

Important dates

Study start
2017
Primary completion
2025
Study completion
2025
First posted
Oct 23, 2017
Registry last updated
Jun 22, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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