Clin2
NCT05462574Possibly a fitRecruiting

MRI study of heart fat in pulmonary arterial hypertension

Idiopathic Pulmonary Arterial HypertensionHeritable Pulmonary Arterial HypertensionPulmonary Arterial Hypertension Associated With Connective Tissue Disease

Part of Lungs & breathing clinical trials.

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.

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

Phase
N/A
Enrollment
75 people
Ages
18 years and older
Study type
Observational

Who can take part

  • You are at least 18 years old
  • You have PAH from an approved cause: idiopathic, inherited, related to connective-tissue disease, or caused by drugs/toxins
  • Your PAH medicines have been stable for the last 3 months (small changes for side effects are allowed)
  • Your PAH symptoms are mild to moderate (WHO functional class I, II, or III), not severe (class IV)
  • You can do all tests: MRI/MRS scan, a 6-minute walk test, and an exercise test
  • You are not pregnant, and you do not need nonstop oxygen

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.

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