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NCT03999138Recruiting

MRI Assessment of Pulmonary Edema in Acute Heart Failure

Source: ClinicalTrials.gov · Last updated 8 May 2026

Brief summary (registry, in English)

Researchers are testing a more accurate way to measure how much fluid is in the lungs (also called pulmonary edema, or "increased lung water") in people with Heart Failure (HF) using MRI (Magnetic Resonance Imaging). There is little known about the exact level of lung water in patients with AHF or how these levels change from the time of hospital admission to discharge. The purpose of this research study is to measure the lung water in patients hospitalized for HF, to determine the change in lung water over the course of hospitalization and treatment, and to find out if lung water levels can predict if patients are higher or lower risk for returning to the hospital or dying from heart failure.

Status (registry)
Recruiting
Study type
Observational
Enrollment
300 (estimated)
First submitted
22 May 2019
Start date
2 Jan 2019
Primary completion date
31 Dec 2027
Lead sponsor
University of Alberta
NCT number
NCT03999138

What you commit to

  • Study type: Observational
  • Planned participants: 300
  • From 2 Jan 2019 to the primary completion date, 31 Dec 2027
  • 2 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • moderate to severe dementia

Other

  • contraindication to MRI
  • patient too critically ill/unstable as per the clinical care team for transport to MRI scanner within the required scanning window

Who the study is looking for

  • 18 years of age or older and willing/able to provide informed consent
  • patients being treated for acute heart failure (including those patients with both reduced and preserved ejection fraction)
  • patients receiving medical therapy for pulmonary edema by current standard of care (including oral or IV diuretics)
  • patients identified within 48 hours of initiation of medical therapy for pulmonary edema, defined as the time of first diuretic (IV or PO) or escalation of existing diuretic therapy administered within the ED or hospital

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University of Alberta
Coordinator of this site? Confirm its status
EdmontonCanadaActive, not recruiting
University of Ottawa Heart Institute
Coordinator of this site? Confirm its status
OttawaCanadaRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.