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A Study of Hemodynamic Cardiopulmonary Exercise for CHD

Not Applicable
Recruiting
Conditions
Congenital Heart Disease
Interventions
Procedure: Cardiac Cath
Registration Number
NCT06566196
Lead Sponsor
Mayo Clinic
Brief Summary

The purpose of this study is to compare the difference in the ability to detect hemodynamic abnormalities between invasive hemodynamic assessments performed at rest versus exercise, to assess the correlation between invasive and noninvasive (Doppler-derived) rest-exercise hemodynamic indices and to compare the association between indices of disease severity and hemodynamic abnormalities identified at rest versus exercise.

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
200
Inclusion Criteria
  • Congenital Heart Disease Diagnosis
  • Undergoing Clinically indicated Cardiac Cath
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Exclusion Criteria
  • Unable to consent
  • Pregnancy
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Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Patients Undergoing Clinically indicated Cardiac CathCardiac Cath-
Primary Outcome Measures
NameTimeMethod
Change in right ventricular free-wall strain from rest to peak exerciseBaseline

Change in right ventricular free-wall strain will be measured in Δ%

Change in pulmonary vascular resistance from rest to peak exerciseBaseline

Change in pulmonary vascular resistance will be measured in ΔWoods Units

Change in left ventricular end-systolic elastance from rest to peak exerciseBaseline

Change in left ventricular end-systolic elastance will be measured in ΔmmHg/mL

Change in systemic vascular resistance from rest to peak exerciseBaseline

Change in systemic vascular resistance will be measured in ΔWoods Units

Change in Left ventricular cardiac output from rest to peak exerciseBaseline

Change in left ventricular cardiac output will be measured in ΔL/min

Change in right ventricular cardiac output from rest to peak exerciseBaseline

Change in right ventricular cardiac output will be measured in ΔL/min

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Mayo Clinic

🇺🇸

Rochester, Minnesota, United States

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