Effects of Pulmonary Hypertension Therapy in Atypical Pulmonary Arterial Hypertension

Overview

Información sobre este estudio

The purpose of this study is to characterize the clinical and hemodynamic response of PAH therapy in patients with atypical PAH and risk factors for left heart disease.

Elegibilidad para la participación

Los requisitos de elegibilidad de los participantes incluyen la edad, el sexo, el tipo y el estadio de la enfermedad, y los problemas de salud o tratamientos previos. Las pautas difieren de un estudio a otro e identifican quiénes pueden o no pueden participar. No hay garantía de que cada persona elegible que desee participar en un ensayo se inscribirá. Comunícate con el equipo del estudio para analizar la elegibilidad del estudio y la posible participación.

Inclusion Criteria:

  • Age ≥ 18 years of age.
  • Precapillary pulmonary hypertension with mean PA pressure > 20 mmHg and planned initiation of pulmonary arterial hypertension therapy.
  • No active treatment for precapillary pulmonary hypertension.
  • Ambulatory (not wheelchair / scooter dependent).
  • Presence of any risk factor for left heart disease will qualify for inclusion (either atrial fibrillation, body mass index > 30 kg/m^2, arterial hypertension, diabetes, coronary artery disease or age > 60 years).

Exclusion Criteria:

  • Significant chronic obstructive pulmonary disease that is a primary contributor to symptoms in the opinion of the investigator.
  • Ischemia thought to contribute to dyspnea in the opinion of the investigator.
  • Obstructive hypertrophic cardiomyopathy.
  • Known infiltrative cardiomyopathy (amyloid).
  • Constrictive pericarditis or tamponade.
  • Active myocarditis.
  • Complex congenital heart disease.
  • More than mild aortic or mitral stenosis.
  • Intrinsic (prolapse, rheumatic) valve disease with more than moderate mitral, tricuspid or aortic regurgitation.
  • Acute or chronic severe liver disease as evidenced by any of the following: encephalopathy, variceal bleeding, INR > 1.7 in the absence of anticoagulation treatment.
  • Terminal illness (other than HF) with expected survival of less than 1 year.
  • Enrollment or planned enrollment in another therapeutic clinical trial in next 3 months.
  • Inability to comply with planned study procedures.
  • Pregnancy or breastfeeding mothers.

Sedes participantes de Mayo Clinic

Los estatus de los estudios cambian con frecuencia. Comunícate con el equipo del estudio para obtener la información más actualizada acerca de la posibilidad de participar.

Sede de Mayo Clinic Estatus Contacto

Rochester, Minn.

Investigador principal de Mayo Clinic

Yogesh Reddy, M.B.B.S.

Cerrado para la inscripción

Contact information:

Louise Durst R.N.

(507) 284-1838

durst.louise@mayo.edu

More information

Publicaciones

Publications are currently not available
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CLS-20508806

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