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Changes in Ischemia and Angina Over 1 Year Among ISCHEMIA Trial Screen Failures With no Obstructive CAD on Coronary CT Angiography (CIAO)

NYU Langone Health logo

NYU Langone Health

Status

Completed

Conditions

Microvascular Angina
Angina Pectoris

Treatments

Other: Quality of Life assessment
Procedure: Stress imaging

Study type

Interventional

Funder types

Other

Identifiers

NCT02347215
s11-00498

Details and patient eligibility

About

Serial assessment of angina status and ischemia on stress echo over one year among patients with moderate ischemia on stress imaging and non-obstructive CAD on coronary CT angiography.

Full description

Some people with chest pain are found to have open arteries on angiograms instead of blocked arteries and many, but not all, of these people have abnormal stress tests or other tests showing there is not enough blood flow to the heart. Prior research has not made clear whether chest pain in such patients is due to heart disease or something else, in part because no one has found out whether chest pain and stress test results change in the same direction over time. This study will use two measurements of chest pain and two stress tests, one year apart, to find out if chest pain and abnormal stress tests are both caused by the same problem: not enough blood flow to the heart.The association between angina, ischemia and atherosclerosis severity at baseline will be examined, as will medication effects.

Enrollment

212 patients

Sex

All

Ages

21 to 100 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Enrolled but not randomized in ISCHEMIA trial
  • Stress echocardiography used for enrollment*
  • No obstructive CAD on study coronary CT angiography (defined as no ≥50% stenosis in a major epicardial vessel)
  • Ischemic symptoms (chest pain or other potential ischemic equivalent).
  • Participant is willing to give written informed consent
  • Age ≥ 21 years

Exclusion criteria

  • Inability to comply with protocol
  • Prior PCI or CABG

Trial design

Primary purpose

Diagnostic

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

212 participants in 1 patient group

All patients
Other group
Description:
All patients undergo quality of life assessment at 2-3 time points and stress imaging at two time points
Treatment:
Procedure: Stress imaging
Other: Quality of Life assessment

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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