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Myocardial Flow Reserve in Severe AS Without Obstructive Coronary Artery Disease

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Samsung Medical Center

Status

Completed

Conditions

Chest Pain
Severe Aortic Stenosis

Treatments

Other: Adenosine-stress cardiac magnetic resonance imaging

Study type

Observational

Funder types

Other

Identifiers

NCT02575768
2012-01-014

Details and patient eligibility

About

Exertional angina is common symptom in patients with severe aortic stenosis (AS) without obstructive coronary artery disease (CAD). Although reduced myocardial flow reserve is one of the proposed explanations for angina, little is known about the pathophysiology.

This study aimed that adenosine-stress cardiac magnetic resonance can be used for the assessment of myocardial perfusion reserve and suggest the pathophysiology of development of angina in patients with severe AS without obstructive CAD.

Enrollment

104 patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  1. severe AS
  2. normal LV ejection fraction (EF ≥ 50%)

Exclusion criteria

  1. age <18
  2. LVEF < 50% in echocardiography
  3. concomitant other valvular disease of moderate or severe severity
  4. previous aortic valve replacement
  5. symptomatic patients other than chest pain
  6. obstructive CAD (>30% luminal stenosis in at least one coronary artery on coronary angiography)
  7. history of myocardial infarction or acute coronary syndrome
  8. contraindication to adenosine
  9. any absolute contraindication to CMR
  10. estimated glomerular filtration rate <30 mL/min/1.73m2.

Trial design

104 participants in 3 patient groups

Severe AS: asymptomatic
Description:
Asymptomatic
Treatment:
Other: Adenosine-stress cardiac magnetic resonance imaging
Severe AS: pure angina
Description:
Presence of exertional chest pain
Treatment:
Other: Adenosine-stress cardiac magnetic resonance imaging
Normal controls
Description:
Healthy controls
Treatment:
Other: Adenosine-stress cardiac magnetic resonance imaging

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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