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Clinical Trials/NCT01318629
NCT01318629UnknownNot Applicable

Invasive Findings in Patients With Angina Equivalent Symptoms But No Coronary Artery Disease; Results From the Heart Quest Cohort Study

Luzerner Kantonsspital1 site in 1 country718 target enrollmentStarted: July 1996Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Enrollment
718
Locations
1
Primary Endpoint
Cause of angina equivalent symptoms in patients with no coronary artery disease

Study Overview

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).

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Coronary angiography at the Luzerner Kantonsspital between July 1st 1996 and July 31st 2008
  • No significant coronary stenoses (no coronary stenoses ≥ 50%)

Exclusion Criteria

  • Severe valvular heart disease
  • Severe congestive heart failure

Outcomes

Primary Outcomes

Cause of angina equivalent symptoms in patients with no coronary artery disease

Time Frame: One day

Prognosis of patients with angina equivalent symptoms and normal coronary arteries

Time Frame: 10 years after baseline assessment

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Prof. Paul Erne

Prof. Paul Erne

Luzerner Kantonsspital

Study Sites (1)

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