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NCT07905443Completed

Bedside Ultrasound in the Emergency Department for Predicting Acute Heart Failure Outcomes

The Role of Point-of-care Ultrasound Protocols in Predicting Clinical Outcomes, Readmission, and Mortality in Patients Presenting to the Emergency Department With Acute Heart Failure

Source: ClinicalTrials.gov · Last updated 29 Oct 2026

Brief summary (registry, in English)

Acute heart failure is a common and serious condition that frequently brings patients to the emergency department. Emergency physicians need quick and reliable methods to evaluate the severity of the condition and monitor the response to initial treatment. This observational study aims to evaluate the effectiveness of bedside ultrasound (Point-of-Care Ultrasound or POCUS) in predicting clinical outcomes for these patients. Researchers will perform bedside ultrasound scans on adult patients presenting with acute heart failure. The scans will be performed twice: first upon admission to the emergency department, and again three hours after starting treatment. The ultrasound protocol will check the heart's pumping ability, look for fluid in the lungs, and measure specific veins (inferior vena cava and internal jugular vein) to assess fluid overload. The main goal of this study is to see if these ultrasound measurements can successfully predict important patient outcomes, including the likelihood of returning to the hospital within 30 days and 30-day survival.

Status (registry)
Completed
Study type
Observational
Enrollment
128 (actual)
First submitted
23 Oct 2026
Start date
11 Oct 2024
Primary completion date
29 May 2025
Lead sponsor
Sakarya University
NCT number
NCT07905443

What you commit to

  • Study type: Observational
  • Participants enrolled: 128
  • From 11 Oct 2024 to the primary completion date, 29 May 2025
  • 1 site 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

  • Presence of interstitial lung disease.
  • Acute renal failure or being on a routine dialysis program.
  • Diagnosis of acute coronary syndrome.
  • Diagnosis of pneumonia or acute exacerbation of chronic obstructive pulmonary disease in the emergency department.

Other

  • Requirement for intubation.
  • Altered mental status / confusion.
  • Pregnancy.
  • Refusal to provide informed consent.

Who the study is looking for

  • Patients presenting to the emergency department with signs and symptoms of acute heart failure.
  • Age older than 18 years.
  • Patients admitted during the working hours of the principal investigator.

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

Full criteria on ClinicalTrials.gov

Sites (1)

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

SiteCityCountrySite status
Sakarya University Training and Research Hospital
Coordinator of this site? Confirm its status
SakaryaTurkey (Türkiye)Unknown status

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