Right Ventricle Lipid in Pulmonary Arterial Hypertension (PAH)
NCT05462574 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 75
Last updated 2025-05-16
Summary
The investigators propose to study the relationship between right ventricle (RV) steatosis and RV function, exercise capacity, and outcomes in humans with pulmonary arterial hypertension (PAH) and to identify potential drivers of lipid accumulation.
Conditions
- Idiopathic Pulmonary Arterial Hypertension
- Heritable Pulmonary Arterial Hypertension
- Pulmonary Arterial Hypertension Associated With Connective Tissue Disease
Interventions
- OTHER
-
No Intervention
No Intervention
Sponsors & Collaborators
-
National Heart, Lung, and Blood Institute (NHLBI)
collaborator NIH -
Vanderbilt University Medical Center
lead OTHER
Principal Investigators
-
Evan Brittain, MD, MSCI · Vanderbilt University Medical Center
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2023-01-17
- Primary Completion
- 2027-09-30
- Completion
- 2027-09-30
Countries
- United States
Study Locations
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