Actively Recruiting

Age: 18Years +
All Genders
NCT06604468

A Portable Thoracic Impedance Device for Detecting Pulmonary Congestion in Heart Failure Patients

Led by Centre hospitalier de l'Université de Montréal (CHUM) · Updated on 2025-10-06

30

Participants Needed

1

Research Sites

52 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This study investigates a portable thoracic bioimpedance tomography (TBIT) device designed to detect early lung congestion in heart failure patients. The main goal is to evaluate how well the device's measurements match those obtained from lung ultrasound and other imaging techniques. By detecting lung fluid build-up before symptoms worsen, this device could help manage heart failure more effectively outside of hospital settings, potentially improving patient care and reducing hospital admissions. Participants in the study are monitored using this device along with standard imaging methods, and data on heart failure symptoms are collected to understand the device\'s accuracy and usability.

CONDITIONS

Official Title

A Portable Thoracic Impedance Device for Detecting Pulmonary Congestion in Heart Failure Patients

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged 18 years or older
  • Diagnosed with heart failure, defined as hospitalization or emergency visit for decompensated heart failure (pulmonary edema) within the last 12 months
Not Eligible

You will not qualify if you...

  • Pregnant women at the time of eligibility evaluation
  • Presence of an implanted electronic device in the thorax, such as a pacemaker or defibrillator
  • Inability to provide informed consent
  • Admission to intensive care or coronary care unit

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

CHUM

Montreal, Quebec, Canada, H2X 3H8

Actively Recruiting

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Research Team

W

William Beaubien-Souligny, MD PhD

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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