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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03911856
Other study ID # 19-000626
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 9, 2020
Est. completion date January 16, 2024

Study information

Verified date March 2024
Source Mayo Clinic
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Researchers are trying to develop innovative strategies that target the early identification heart and lung imbalances in patients with cardiopulmonary diseases.


Recruitment information / eligibility

Status Completed
Enrollment 7
Est. completion date January 16, 2024
Est. primary completion date January 16, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion criteria: - Healthy controls (no known cardiac or pulmonary disease); - PAH/HFpEF patients with known RV failure; - PAH/HFpEF patients with known pulmonary failure - Newly diagnosed PAH/HFpEF patients without any evidence of profound RV or pulmonary dysfunction. Exclusion criteria: - Persons unable to perform light exercise - Persons pregnant or planning to be pregnant

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Echocardiography
We hypothesize that non-invasive indices of RV (echocardiograph-derived strain and strain rate) and pulmonary (gas exchange-derived lung diffusion and surface area) function during light exercise will successfully identify and discern patients with known RV dysfunction (PAH/HFpEF with RV failure) from those with known pulmonary dysfunction (PAH/HFpEF with pulmonary fibrosis). Additionally, we hypothesize that our assessment techniques will identify subtle derangements in RV and pulmonary function in newly diagnosed PAH and HFpEF patients, and that this may guide early and targeted therapeutic intervention.
Pulmonary Gas Exchange
We hypothesize that breathing hyperoxia will increase exercise capacity by reversing RV and pulmonary derangements, and that the mechanisms of action will be related to the underlying dysfunction (e.g., reducing PVR, increasing RV functional reserve, increasing gas diffusion).

Locations

Country Name City State
United States Mayo Clinic in Rochester Rochester Minnesota

Sponsors (1)

Lead Sponsor Collaborator
Mayo Clinic

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in stroke volume (SV) during exercise and hyperoxia Stroke volume will be measured with echocardiography at rest and during exercise while breathing room air and hyperoxia 2 years
Primary Change in oxygen uptake (VO2) during exercise and hyperoxia Oxygen uptake will be measured via pulmonary gas exchange at rest and during exercise while breathing room air and hyperoxia 2 years
Primary Change in ventilatory efficiency (VE/VCO2) during exercise and hyperoxia Ventilatory effciency will be measured via pulmonary gas exchange at rest and during exercise while breathing room air and hyperoxia 2 years
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