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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT00548457
Other study ID # SHEBA-06-4130-PC-CTIL
Secondary ID
Status Recruiting
Phase N/A
First received October 23, 2007
Last updated January 28, 2008
Start date May 2006

Study information

Verified date January 2008
Source Sheba Medical Center
Contact ARIK ASMAN, MD
Phone 972-3-5302454
Email asman@sheba.health.gov.il
Is FDA regulated No
Health authority Israel: Israeli Health Ministry Pharmaceutical Administration
Study type Observational

Clinical Trial Summary

The aim of this study is to show the frequency of endothelial dysfunction in patients suffering from ectatic coronary arteries as compared to those who have normal coronary arteries. Should this frequency be significant we would recommend initiating conventional treatment in those patients with ectatic coronary arteries as is the practice in patients with endothelial dysfunction without ectatic arteries


Recruitment information / eligibility

Status Recruiting
Enrollment 76
Est. completion date
Est. primary completion date
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 90 Years
Eligibility Inclusion Criteria:

- Ectatic coronary arteries defined by cardiac catheterization

Study Design

Observational Model: Case Control, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
Israel Heart Institute, Chaim Sheba Medical Center Tel Hashomer

Sponsors (1)

Lead Sponsor Collaborator
Sheba Medical Center

Country where clinical trial is conducted

Israel, 

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