CArdioMEtabolic Function and Reserve Capacity in Healthy Adults

Overview

Información sobre este estudio

The purpose of this study is to evaluate pulmonary capillary wedge pressure (PCWP) and other hemodynamic measurements at rest and during exercise in healthy volunteers across the age spectrum.

 

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:

  • Healthy volunteers are eligible to participate in this study if they have are free of symptoms of exertional breathlessness or fatigue and any diagnosis of heart failure.  
  • Patients will also be required to have left ventricular EF ≥ 50%.  
  • Patients discovered to reduced EF or abnormal resting hemodynamics or other pathologic findings previously undiscovered will be considered screen failures and can be replaced by others to reach the goal enrollment.
  • Informed consent were obtained.
  • Age ≥ 18 years at the time of signing informed consent.
  • No history of heart failure.
  • Willing and able to undergo invasive hemodynamic exercise testing, MRI, and other study assessments.

Exclusion Criteria:

  • Clinically significant symptoms of exertional dyspnea or fatigue in daily life in the opinion of the investigators.
  • Any diagnosis of heart failure.
  • Symptomatic coronary artery disease (e.g., patients with chronic angina).
  • Symptomatic valvular heart disease.
  • Pulmonary hypertension.
  • Cardiomyopathies.
  • High output heart failure.
  • Pericardial disease.
  • Clinically significant chronic lung disease in the opinion of the investigators.
  • Anemia (hemoglobin < 12 gm/dL in women and < 13 gm/dL in men).
  • Estimated glomerular filtration rate < 60.
  • Pregnant women.
  • Any other disorders or problems that would interfere with the ability to participate safely in the study (e.g. psychiatric disorder or substance abuse).

Note: Other protocol defined Inclusion/Exclusion Criteria may apply.

Eligibility last updated 7/24/23. Questions regarding updates should be directed to the study team contact.

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

Barry Borlaug, M.D.

Comunícate con nosotros para obtener el estatus más reciente

Contact information:

RST Borlaug Study Team

(507) 255-2200

More information

Publicaciones

Publications are currently not available
.
CLS-20560506

Mayo Clinic Footer