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Clinical Trials/NL-OMON42844
NL-OMON42844
Completed
Not Applicable

Microvascular Function in Non-ST-segment Elevation Acute Coronary Syndrome - DEFINE NSTEMI

Academisch Medisch Centrum0 sites60 target enrollmentTBD

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
microvascular dysfunction
Sponsor
Academisch Medisch Centrum
Enrollment
60
Status
Completed
Last Updated
2 years ago

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
2 years ago
Study Type
Observational invasive

Investigators

Eligibility Criteria

Inclusion Criteria

  • 1\. Stable angina (CCS class I to III, or Braunwald class I) or NSTE\-ACS (Chest pain within the preceding 5 days and an index event \>24 hours from time of angiography but within the previous 7 days).;2\. Scheduled for percutaneous coronary intervention or intracoronary evaluation of functional stenosis severity (diagnostic catheterization).;3\. The presence of at least one normal or minimally diseased reference coronary artery (\<30% diameter stenosis on visual assessment) with a vessel diameter of more than 2\.5 mm.

Exclusion Criteria

  • 1\. Younger than 19 or older than 80 years of age.;2\. Recent ST\-segment elevation myocardial infarction (\<6 weeks prior to enrollment).;3\. Inability to receive intravenous adenosine (for example, severe reactive airway disease, marked hypotension, or high\-grade AV block without pacemaker).;4\. Known renal insufficiency (eGRF according to MDRD \<30 mL/min/m2\).;5\. Known severe valvular abnormalities.;6\. Known severe left ventricular dysfunction (LV ejection fraction \<30%) or known myocardial hypertrophy (septal wall thickness at echocardiography of \>13 mm).;7\. Extremely tortuous or calcified coronary arteries precluding intracoronary physiologic measurements.;8\. Women of child bearing age not on active birth control;9\. Inability to sign an informed consent, due to any mental condition that renders the subject unable to understand the nature, scope, and possible consequences of the trial or due to mental retardation or language barrier.

Outcomes

Primary Outcomes

Not specified

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