Stress Echo 2030

Overview

About this study

This study (SE2030) will establish a platform of data to build the perfect stress echo test, suitable for all patients, anywhere, anytime, also quantitative and operator independent.

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria:

  • Age 18+.
  • Undergoing a clinically indicated stress echo, Capacity to consent.
  • Prior diagnosis of the following:
  • Coronary Artery Disease
    • Undergoing SE for one of the following indications:
      • For Assessment of chest pain or dyspnea;
      • For reassessment after an abnormal test or assessment of known CAD (previous acute coronary syndrome and/or previous myocardial revascularization, prior CAD by invasive or noninvasive coronary angiography);
      • For risk stratification prior to high risk non-cardiac vascular surgery (such as liver transplant or major non-cardiac vascular surgery) in patients with poor functional capacity (< 4 METS) and/or suspected cardiac symptoms, in presence of a revised cardiac risk index (Lee criteria)  ≥ 2 (high risk surgery;
      • CAD;
      • congestive heart failure;
      • cerebrovascular disease;
      • diabetes mellitus on insulin;
      • serum creatinine > 2mg/ml).
  • Diastolic Heart Failure
    • Preserved EF;
    • Heart Failure score 1-5.
  • Hypertrophic Cardiomyopathy
    • Phenocopies such as infiltrative/ storage disease (e.g., Fabry, amyloid) will be excluded.
  • Post Chest Radio/Chemotherapy.
  • Tetralogy of Fallot (TOF)
    • Repaired TOF, double-outlet right ventricle Fallot type, tetralogy of Fallot with pulmonary atresia;
    • At least 1 year post-surgical or percutaneous procedure
    • Height > 140 cm;
    • New York Heart Association class I or II.
  • Mitral Regurgitation
    • Resting moderate mitral regurgitation (effective regurgitant orifice 0.2-0.39 cm^2, and regurgitant volume 30-59 ml) of ischemic origin.
  • Valvular Heart Disease
    • Asymptomatic severe aortic stenosis;
    • Low-flow, low-gradient aortic stenosis with reduced ejection fraction;
    • Low-flow, low-gradient aortic stenosis with preserved ejection fraction;
    • Asymptomatic severe or symptomatic non-severe primary mitral insufficiency;
    • Asymptomatic severe or symptomatic non-severe aortic regurgitation;
    • Asymptomatic severe or symptomatic non-severe mitral stenosis;
    • Asymptomatic severe or symptomatic non-severe multivalvular disease;
    • Post heart valve procedures (prostheses and valvuloplasty).

Exclusion Criteria: 

  • Under the age of 18.
  • Unable to consent.

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status Contact

Rochester, Minn.

Mayo Clinic principal investigator

Patricia Pellikka, M.D.

Open for enrollment

Contact information:

Halley Davison

(507) 422-6246

davison.halley@mayo.edu

More information

Publications

Publications are currently not available
.
CLS-20543049

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