- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00548457
Endothelial Function in Patients With Ectatic Compared to Normal Coronary Arteries
January 28, 2008 updated by: Sheba Medical Center
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
Study Overview
Status
Unknown
Conditions
Study Type
Observational
Enrollment (Anticipated)
76
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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-
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Tel Hashomer, Israel, 52621
- Recruiting
- Heart Institute, Chaim Sheba Medical Center
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Contact:
- Micahel Shechter, MD, MA
- Phone Number: 972-3-5302645
- Email: shechter@sheba.health.gov.il
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Principal Investigator:
- Arik Asman, MD
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Sub-Investigator:
- Pierre Chouraqui, MD
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Sub-Investigator:
- Michael Shechter, MD
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
14 years to 86 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
Patients were recruited after passing cardiac catherization and diagnosed as having ectatic arteries.
Description
Inclusion Criteria:
- Ectatic coronary arteries defined by cardiac catheterization
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Observational Models: Case-Control
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
|---|
|
A
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Chair: Pierre Chouraqui, MD, Sheba Medical Center
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
May 1, 2006
Study Registration Dates
First Submitted
October 23, 2007
First Submitted That Met QC Criteria
October 23, 2007
First Posted (Estimate)
October 24, 2007
Study Record Updates
Last Update Posted (Estimate)
January 29, 2008
Last Update Submitted That Met QC Criteria
January 28, 2008
Last Verified
January 1, 2008
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- SHEBA-06-4130-PC-CTIL
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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