Clin2
NCT05584722Possibly a fitRecruiting

Study risk and resilience in pulmonary arterial hypertension

Idiopathic Pulmonary Arterial HypertensionHeritable Pulmonary Arterial HypertensionUnaffected Mutation Carriers: Healthy Participants With a Known BMPR2 Gene Mutation and Normal Pulmonary Pressure and RV Function on EchoHealthy Individuals With no Cardiopulmonary Disease

Part of Heart & circulation, Lungs & breathing clinical trials.

This study looks at how people with pulmonary arterial hypertension (PAH) and certain genetic risks cope and how their bodies respond over time. It may help researchers understand factors linked to better or worse outcomes, and how different people manage the condition.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
150 people
Ages
15 years to 80 years
Study type
Observational

Who can take part

  • You are between 15 and 80 years old
  • You either have idiopathic or heritable PAH, or you are a healthy person with a known BMPR2 gene change
  • Your heart and lung symptoms are mild to moderate (WHO functional class I to III), not severe (class IV)
  • If you have PAH, your PAH medicines have been stable for 3 months (at most one diuretic change; more than two likely excludes you)
  • You are not pregnant

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

Similar studies

Other trials that look related to this one.

NCT01884051Recruiting
Study of blood and skin changes in pulmonary hypertension

This study looks at how hormones, metabolism, and body signals relate to pulmonary arterial hypertension. You may be eligible if you (or a family member) have idiopathic, inherited, or related pulmonary arterial hypertension, and you can do required blood and other testing.

Nashville, Tennessee
NCT05462574Recruiting
MRI study of heart fat in pulmonary arterial hypertension

This trial uses MRI (and an additional MRI measurement called MRS) to study fat in the right side of the heart in people with pulmonary arterial hypertension (PAH). It may help researchers understand what’s going on in PAH and how it relates to symptoms and exercise ability.

Nashville, Tennessee
NCT05464095Recruiting
Mobile health support for pulmonary arterial hypertension

This study tests whether using a mobile health tool can help people with pulmonary arterial hypertension (PAH) manage their condition in daily life. It’s aimed at adults who are stable on their PAH medicines and can track activity using a wearable device.

Nashville, Tennessee
NCT01730092Recruiting
Study of blood and imaging biomarkers in pulmonary artery hypertension

This study tracks natural changes in “biomarkers” (measurable signals in blood) and imaging findings in people with pulmonary arterial hypertension (PAH) or suspected PAH. It also includes healthy people for comparison, helping researchers understand what these signals mean over time.

Bethesda, Maryland
NCT07131241Recruiting
A study to predict risk in pulmonary hypertension

This study aims to better predict the future risk for people with pulmonary hypertension (high blood pressure in the lungs) by combining different types of health information collected over time. If you join, researchers will track your health data to build a tool that personalizes care and improves outcomes.

Fuzhou, Fujian
NCT05368467Recruiting
Registry study for pulmonary hypertension patients

This is a long-term study that enrolls people who have been diagnosed with pulmonary hypertension (high blood pressure in the lung arteries). It collects medical information over time to better understand the condition and what to expect.

Guangzhou, Guangdong

Hear when a new Idiopathic Pulmonary Arterial Hypertension trial opens

We’ll email you when one opens — at most once a week, no account needed, unsubscribe anytime.