Researchers dive into why scleroderma and lung hypertension weaken the heart
NCT ID NCT04610788
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looked at 43 adults with scleroderma or unexplained pulmonary arterial hypertension (PAH) to understand why the right side of the heart weakens. Researchers collected blood and tissue samples during routine procedures and measured heart function over 6 months. The goal was to learn how standard PAH treatment affects the heart, not to test a new therapy.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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43 people
The number who actually took part.
- Started
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Apr 2019
- Finished
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Dec 2025
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Patients 18 years or older with clinically diagnosed scleroderma or presumed/known idiopathic pulmonary hypertension.
- Ages
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18 to 100 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Patients 18 years or older with clinically diagnosed scleroderma or presumed/known idiopathic pulmonary hypertension. Exclusion Criteria: * Patients found to have secondary pulmonary hypertension (PH due to left heart failure) on clinical RHC. * Hemodynamically unstable patients (systolic blood pressure \< 90mmHg, vasopressor requirement). * Patients whom are unable to give consent for themselves. * Patients with RV clot or septal aneurysm will be excluded. * In order to undergo the clinical right heart catheterization procedures, pregnancy testing (urine or serum) is standard of care. * Pregnancy
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Johns Hopkins
Baltimore, Maryland, 21287, United States
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Other studies related to the condition(s) this trial covers.
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