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Completed

NCT Number: NCT01365806

Home Electrocardiogram (ECG) Monitoring After Heart Transplantation

The long-term goal of this research is to apply novel technology for detection of donor organ (allograft) rejection to improve patient outcomes following heart transplantation. The specific goal of this study is to determine whether daily monitoring of the transplant recipient's electrocardiogram (ECG) using a simple home device with transmission to an ECG Core Laboratory would provide an early biomarker for acute rejection. Despite routine immunosuppressant drug therapy, acute rejection is common, especially within the first 6 months following transplant surgery. To detect rejection, frequent endomyocardial biopsies of heart tissue are performed. An endomyocardial biopsy is a costly and invasive procedure performed in a hospital cardiac catheterization laboratory that has associated risks. Recent evidence suggests that acute allograft rejection causes delays in ventricular repolarization resulting in a longer QT interval on the ECG. The specific aims of the study are to: 1) determine whether an increase in the QT interval during the first 6 months following heart transplant is a sensitive and specific biomarker for acute rejection; and 2) determine the timing of QT interval increases relative to biopsy-diagnosed stages of mild/moderate/severe rejection. The potential benefit of finding a simple ECG biomarker of allograph rejection that could be measured at home is that it might yield earlier detection of rejection, allow more timely therapy and reduce mortality from acute allograft rejection.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Cedars-Sinai Medical Center, Los Angeles, California, United States

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Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • ≥18 years of age
  • first heart transplant surgery
  • not enrolled in other research studies that conflict with study design

Exclusion criteria

  • clinically unstable at time of enrollment (i.e. clinical symptoms of allograph impairment)

Treatment and study plan

Primary outcomes

  1. number and grade of acute allograft rejection episodes

    Time frame: within one year after transplant surgery

Secondary outcomes

  1. all cause mortality

    Time frame: one year after transplant surgery

Sponsors and collaborators

Lead sponsor

University of California, Los Angeles

Other

Collaborators

  • Cedars-Sinai Medical Center
  • Columbia University
  • National Institute of Nursing Research (NINR)
  • University of California, San Francisco

Registry information

Official study title

Home ECG Monitoring to Detect Allograft Rejection Following Heart Transplantation

Acronym: NEW HEART

Important dates

Study start
2011
Primary completion
2015
Study completion
2016
First posted
Jun 3, 2011
Registry last updated
Mar 8, 2017

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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