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Angina in Non Coronary Artery Disease

Conditions
Angina Pectoris
Microvascular Angina
Angina Pectoris, Variant
Registration Number
NCT01318629
Lead Sponsor
Luzerner Kantonsspital
Brief Summary

Many patients undergoing coronary angiography are found to have no significant coronary artery disease (CAD) despite angina equivalent symptoms and/or electrocardiographic abnormalities suggestive of myocardial ischemia. The aim of this study is to systematically assess patients with angina equivalent symptoms despite normal coronary angiograms and to evaluate their symptoms according to a defined algorithm.

Detailed Description

All consecutive patients who had coronary angiography at the Luzerner Kantonsspital between July 1st 1996 and July 31st 2008 and who had no significant coronary stenoses (no coronary stenoses ≥ 50%) were recruited for this study. Patients are extensively examined during angiography using acetylcholine infusion and fast atrial pacing. According to the result of the additional invasive examination (vasospasm, vasoconstriction, vasodilation; symptoms during examination) a distinct diagnosis is attributed to the patients (small vessel disease, vasospastic disease, hypertensive heart disease, rhythm disorder, or extracardiac thoracic pain including pulmonary hypertension). Patients are followed-up after 10 years and prognosis of these patients is assessed (including mortality, cardiovascular events, re-angiography, functional status after 10 years).

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
718
Inclusion Criteria
  • Coronary angiography at the Luzerner Kantonsspital between July 1st 1996 and July 31st 2008
  • No significant coronary stenoses (no coronary stenoses ≥ 50%)
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Exclusion Criteria
  • Severe valvular heart disease
  • Severe congestive heart failure
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Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Cause of angina equivalent symptoms in patients with no coronary artery diseaseOne day
Prognosis of patients with angina equivalent symptoms and normal coronary arteries10 years after baseline assessment
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Luzerner Kantonsspital

🇨🇭

Luzern, Switzerland

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