Using contrast echocardiography during exercise to assess pulmonary blood volume
Official title: Assessment of Pulmonary Blood Volume Using Contrast Echocardiography During Exercise
Run by Mayo Clinic · NCT06195059 · Data updated 2026-11-12
This study is testing if a special heart ultrasound can safely measure blood volume in the lungs during exercise to help understand how it affects people with and without heart failure.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 800 (estimated) |
| Sponsor | Mayo Clinic Academic / other |
| Locations | 1 site (Rochester, Minnesota) |
| Status | Recruiting |
| Started | July 30, 2024 |
| Main results expected | August 2027 |
| Study ends | August 2027 |
| Registry record updated | August 20, 2026 |
| Trial ID | NCT06195059 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates include patients referred for invasive exercise right heart catheterization who experience exertional dyspnea and have varying degrees of pulmonary hypertension.
✕Probably not a fit
Patients who are unable or unwilling to undergo echocardiography or have had prior adverse reactions to echo contrast administration may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This observational study aims to evaluate the effectiveness of pulmonary blood volume (PBV) measurements obtained through contrast echocardiography as a non-invasive alternative to invasive pulmonary artery wedge pressure (PAWP) during exercise. It will compare changes in PBV in patients with and without heart failure and pulmonary vascular disease. The study will involve patients referred for invasive exercise right heart catheterization due to exertional dyspnea, allowing for a comprehensive assessment of PBV in relation to exercise performance.
Why it matters
Potential benefit: If successful, this study could provide a safer, non-invasive method for assessing pulmonary blood volume in patients with heart failure and pulmonary vascular disease.
How similar studies have gone: While this approach is innovative, it builds on existing methodologies in echocardiography, and similar studies have shown promise in non-invasive assessments of cardiac function.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patients referred to the cardiac catheterization laboratory for invasive exercise right heart catheterization for evaluating exertional dyspnea. Investigators will include patients with normal or low EF, and across the spectrum of pulmonary hypertension severity. Exclusion Criteria: * Patient inability or unwillingness to undergo echocardiography including a contrast method, or if echocardiography would, in the opinion of the investigator, somehow compromise the quality of data acquisition for the clinical case. * Prior adverse reaction to echo contrast administration
Where it's running
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Mayo Clinic in Rochester
Rochester, Minnesota, United States Recruiting
Study contacts
- Principal investigator: Barry Borlaug, MD — Mayo Clinic
- Study coordinator: Circulatory Failure Research Team
- Phone: 507-255-2200
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.