Fact CheckerSign in

NCT00823563Recruiting

Evaluation of Patients With Non-obstructive Coronary Arteries

Evaluation of Patients With Angina in the Absence of Obstructive Coronary Artery Disease

Source: ClinicalTrials.gov · Last updated 5 Jun 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

Patients with angina and non-obstructive CAD are common within clinical practice, but remain a challenge with regard to diagnosis and treatment. When these patients undergo a comprehensive evaluation at the time of invasive coronary angiography, occult coronary abnormalities are frequently found. We hope to learn the overall prevalence and presentation of these occult coronary abnormalities and its long term outcome in this patient population.

Status (registry)
Recruiting
Study type
Observational
Enrollment
2000 (estimated)
First submitted
14 Jan 2009
Start date
1 Jun 2007
Primary completion date
30 Jun 2047
Lead sponsor
Stanford University
NCT number
NCT00823563

What you commit to

  • Study type: Observational
  • Planned participants: 2000
  • From 1 Jun 2007 to the primary completion date, 30 Jun 2047
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Currently taking vasoactive medication (such as nitroglycerin)

Other illness

  • Status-post heart transplant
  • Presence of another likely explanation of chest pain, such as pulmonary hypertension or aortic stenosis
  • History of adverse reaction to any of the medications being used (acetylcholine, nitroglycerin, adenosine, or heparin)
  • A hearing impairment that won't allow for a typical verbal conversation or a visual impairment that won't allow for reading of the written consent

Lab values

  • Renal insufficiency (creatinine \>1.5)
  • Presence of an acute coronary syndrome (STEMI or NSTEMI), Tako-tsubo, an abnormal ejection fraction (EF\<55%), cardiogenic shock, or recent VT/VF

Age

  • Age \<18

Other

  • Asymptomatic (such as a pre-op cath)
  • Inability to provide an informed consent, including an inability to speak, read, or understand English, Spanish, Chinese, Farsi, Japanese, Korean, Russian, or Vietnamese
  • Participation in another study (with the exception of the Stanford Gene-PAD study)
  • A potentially vulnerable subject (including minors, pregnant women, economically and educationally disadvantaged, decisionally impaired, and homeless people)

Who the study is looking for

  • Patient referred for elective coronary angiography because of a reasonable clinical suspicion of coronary ischemia.
  • Presence of angina or an anginal equivalent (including chest, back, shoulder, arm, neck, jaw discomfort, or shortness of breath brought on by physical exertion, emotional stress, or certain times of day/month).

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Stanford University School of Medicine
Coordinator of this site? Confirm its status
StanfordUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.