Completed

Phase 3
Age: 15Years +
FEMALE
ID00000554

Led by University of Pittsburgh · Updated on 2014-04-04

N/A

Participants Needed

N/A

Research Sites

N/A

Total Duration

On this page

Sponsors

U

University of Pittsburgh

Lead Sponsor

N

National Heart, Lung, and Blood Institute (NHLBI)

Collaborating Sponsor

AI-Summary

What this Trial Is About

To evaluate innovative diagnostic methods that will improve the diagnostic reliability of cardiovascular testing in evaluation of ischemic heart disease in women. Innovative approaches proposed include physiologic or functional measurements such as impaired metabolism, perfusion, or endothelial function as well as assessment of epicardial coronary arteries by angiography. Other objectives include developing safe, accurate, and cost effective diagnostic approaches for evaluating women with suspected ischemic heart disease, and determining the frequency of myocardial ischemia in the absence of significant epicardial coronary stenosis, as well as the frequency of non-ischemic or non-cardiac chest pain. A key aspect of the WISE study is to determine whether evidence of myocardial ischemia occurs in the absence of obstructive coronary disease.

CONDITIONS

Official Title

Women's Ischemia Syndrome Evaluation (WISE)

Who Can Participate

Age: 15Years +
FEMALE

Eligibility Criteria

Eligible

You may qualify if you...

Women over the age of 18 who have suspected ischemic heart disease.

Not Eligible

You will not qualify if you...

History of severe allergic reactions to study medication Currently pregnant or breastfeeding Recent participation in another clinical trial within the last 30 days Presence of uncontrolled medical conditions that could affect safety

Trial Site Locations

Site Locations not provided

Location information for this trial is currently unavailable.

How is the study designed?

Study Type

INTERVENTIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

DIAGNOSTIC

Number of Arms

0

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Published Research Related To This Trial

Coronary flow velocity response to adenosine characterizes coronary microvascular function in women with chest pain and no obstructive coronary disease. Results from the pilot phase of the Women's Ischemia Syndrome Evaluation (WISE) study.

S E Reis, R Holubkov, J S Lee...

https://pubmed.ncbi.nlm.nih.gov/10334410

Dobutamine stress echocardiography in women with chest pain. Pilot phase data from the National Heart, Lung and Blood Institute Women's Ischemia Syndrome Evaluation (WISE).

J F Lewis, L Lin, S McGorray...

https://pubmed.ncbi.nlm.nih.gov/10334409

Effect of coronary angiography on use of lipid-lowering agents in women: a report from the Women's Ischemia Syndrome Evaluation (WISE) study. For the WISE Investigators.

V Bittner, M Olson, S F Kelsey...

https://pubmed.ncbi.nlm.nih.gov/10781756

Weight cycling and high-density lipoprotein cholesterol in women: evidence of an adverse effect: a report from the NHLBI-sponsored WISE study. Women's Ischemia Syndrome Evaluation Study Group.

M B Olson, S F Kelsey, V Bittner...

https://pubmed.ncbi.nlm.nih.gov/11079659

Detailed angiographic analysis of women with suspected ischemic chest pain (pilot phase data from the NHLBI-sponsored Women's Ischemia Syndrome Evaluation [WISE] Study Angiographic Core Laboratory).

B L Sharaf, C J Pepine, R A Kerensky...

https://pubmed.ncbi.nlm.nih.gov/11305981

Coronary microvascular dysfunction is highly prevalent in women with chest pain in the absence of coronary artery disease: results from the NHLBI WISE study.

S E Reis, R Holubkov, A J Conrad Smith...

https://pubmed.ncbi.nlm.nih.gov/11320360

History of anxiety disorders is associated with a decreased likelihood of angiographic coronary artery disease in women with chest pain: the WISE study.

T Rutledge, S E Reis, M Olson...

https://pubmed.ncbi.nlm.nih.gov/11693752