Actively Recruiting
Invasive Hemodynamic Cardiopulmonary Exercise Testing for Assessment of Patients With Congenital Heart Disease
Led by Mayo Clinic · Updated on 2026-03-05
200
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
Sponsors
M
Mayo Clinic
Lead Sponsor
N
National Heart, Lung, and Blood Institute (NHLBI)
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are evaluating the ability to detect blood flow and heart function abnormalities in patients with congenital heart disease using invasive hemodynamic assessments at rest and during exercise. The study aims to compare how well invasive measurements match noninvasive Doppler methods and to see how these measurements relate to disease severity. This research is sponsored by the Mayo Clinic and focuses on improving assessment techniques for congenital heart disease. Participants will undergo a standard cardiac catheterization procedure alongside an invasive cardiopulmonary exercise test during the same procedure. This combined testing will measure heart and blood vessel function at rest and during peak exercise to capture changes in heart muscle stiffness, cardiac output, vascular resistance, and strain on the right ventricle. The intervention involves one study group consisting of patients undergoing clinically indicated cardiac catheterization with the added exercise testing. During the study, participants will be closely monitored through invasive measurements collected during their catheterization and exercise testing. Researchers will evaluate changes from rest to peak exercise in multiple heart function indicators, including left and right ventricular output, systemic and pulmonary vascular resistance, and ventricular strain. The study will last until December 2026, and the data collected will help understand heart function during exercise in congenital heart disease patients.
CONDITIONS
Brief Title
A Study of Hemodynamic Cardiopulmonary Exercise for CHD
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Diagnosis of congenital heart disease
- Scheduled for a clinically indicated cardiac catheterization
- Age 18 years or older
- Ability to provide informed consent
You will not qualify if you...
- Unable to provide consent
- Pregnancy
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 1 day
Participants undergo invasive cardiopulmonary exercise testing during a clinically indicated cardiac catheterization procedure.
1 visit (in-person)
Trial Site Locations
Total: 1 location
1
Mayo Clinic
Rochester, Minnesota, United States, 55905
Actively Recruiting
Research Team
A
ACHD Research Program
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
DIAGNOSTIC
Number of Arms
1
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