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The Cardiovascular Effects of Patent Foramen Ovale in Hypoxia

The Role of Patent Foramen Ovale on Cardiac Hemodynamics and Exercise Cardiac Reserve in HAPE-susceptible Individuals

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07742540
Enrollment
50
Registered
2026-08-03
Start date
2026-09-15
Completion date
2028-09-15
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

High Altitude Pulmonary Edema, Patent Foramen Ovale (PFO)

Keywords

hypoxia, altitude, heart, high altitude pulmonary edema, patent foramen ovale, exercise, pulmonary artery pressure, intracardiac pressures, right-to-left shunt

Brief summary

Before birth, the foramen ovale is a normal opening in the heart that allows blood to flow from the mother to the baby. After birth, this opening usually closes. However, in up to 38% of the population it does not fully close and is then called a patent foramen ovale (PFO). Having a PFO allows venous (blue) blood to mix with arterial (red) blood in the heart, which can lower blood oxygen levels. The mixing of blood has been suggested to be greater during exercise and with exposure to high-altitude. Also, people with a PFO may be a greater risk for severe altitude sickness, specifically involving the collection of fluid in the lungs which makes breathing very difficult - this is called high-altitude pulmonary edema (HAPE). No study has directly measured the pressure difference across the heart which is required for the mixing of blood during exercise or at high-altitude. The present study will directly measure the pressure difference across the heart, as well as blood flow through the PFO during rest and exercise in simulated high altitude in adults with and without a PFO and a previous history of severe altitude sickness. The study will test the hypothesis that elevations in pulmonary artery pressure during exposure to hypoxia will not elicit a pressure gradient, and thus blood flow, across the PFO neither at rest nor during exercise.

Interventions

None listed

Sponsors

University of Texas Southwestern Medical Center
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
Yes

Inclusion criteria

* Males and females age \> 18 but \< 60 years of age at the time of signing the informed consent. * Medically documented episode of noncardiogenic pulmonary edema occurring after exposure to hypoxia at high altitude. * No other associated congenital cardiac or vascular abnormalities. * Physically active, and able to perform endurance exercise.

Exclusion criteria

* Do not otherwise meet the inclusion criteria. * Cardiac- or pulmonary-related medications. * Known history of anemia, iron deficiency, iron supplementation (oral or intravenous) in the preceding 60 days. * Systemic anticoagulation or aspirin use that cannot be temporarily held for the study. * Non-cardiopulmonary disorders that adversely influence exercise ability (e.g. arthritis or peripheral vascular disease). * Engaging in vigorous physical activity \[≥1 hour at ≥6 mets\] at ≥8,000 ft for \>2 days per week over the preceding 4 weeks, and residing at ≥8,000 ft for 3 or more consecutive nights in the preceding 30 days. * History of any recent illnesses (e.g. viral respiratory infections) within 4 weeks of testing. * Women who are pregnant (urine pregnancy test given to all women of childbearing age at the time of testing). * Other conditions that would limit the patient's ability to complete the study procedures.

Design outcomes

Primary

MeasureTime frameDescription
Transmural pressureDuring 5 minutes of rest in normoxia, after 15 minutes of exercise in normoxia, after 90 minutes of rest in hypoxia, after 15 minutes of exercise in hypoxia.Absolute difference between pulmonary capillary wedge pressure and right atrial pressure
Arterial oxygen saturationDuring 5 minutes of rest in normoxia, after 15 minutes of exercise in normoxia, after 90 minutes of rest in hypoxia, after 15 minutes of exercise in hypoxia.
Pulse oxygen saturationDuring 5 minutes of rest in normoxia, after 15 minutes of exercise in normoxia, after 90 minutes of rest in hypoxia, after 15 minutes of exercise in hypoxia.

Secondary

MeasureTime frameDescription
Gas exchangeDuring 5 minutes of rest in normoxia, after 15 minutes of exercise in normoxia, after 90 minutes of rest in hypoxia, after 15 minutes of exercise in hypoxia.Oxygen uptake and carbon dioxide production
Arterio-venous oxygen differentDuring 5 minutes of rest in normoxia, after 15 minutes of exercise in normoxia, after 90 minutes of rest in hypoxia, after 15 minutes of exercise in hypoxia.
Cardiac outputDuring 5 minutes of rest in normoxia, after 15 minutes of exercise in normoxia, after 90 minutes of rest in hypoxia, after 15 minutes of exercise in hypoxia.
Right ventricular diameterDuring 5 minutes of rest in normoxia, after 15 minutes of exercise in normoxia, after 90 minutes of rest in hypoxia, after 15 minutes of exercise in hypoxia.
Tricuspid regurgitant jet velocityDuring 5 minutes of rest in normoxia, after 15 minutes of exercise in normoxia, after 90 minutes of rest in hypoxia, after 15 minutes of exercise in hypoxia.
Tricuspid annular plane systolic excursionDuring 5 minutes of rest in normoxia, after 15 minutes of exercise in normoxia, after 90 minutes of rest in hypoxia, after 15 minutes of exercise in hypoxia.

Contacts

CONTACTGiorgio Manferdelli, Ph.D.
giorgio.manferdelli@utsouthwestern.edu214-345-7134
CONTACTMary Childers
marychilders@texashealth.org214-345-6459
PRINCIPAL_INVESTIGATORBenjamin D. Levine, M.D.

The University of Texas Southwestern Medical Center Dallas

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 4, 2026