Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID06566196

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

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Diagnostic Evaluation

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

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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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