- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00918242
Prevalence of Coronary Artery Disease in the Siblings of Premature Coronary Heart Disease
July 20, 2012 updated by: Hyuk-Jae Chang, Yonsei University
Assessment of Occult CAD: Premature CAD Sibling Study (PreCASS)
The aim of this prospective study is to investigate the prevalence of coronary artery disease using computed tomography with family history of premature coronary heart disease
Study Overview
Status
Unknown
Conditions
Study Type
Observational
Enrollment (Anticipated)
87
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Hyuk-Jae Chang, MD, PhD
- Phone Number: 82-2-2228-8461
- Email: hjchang@yuhs.ac
Study Locations
-
-
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Seoul, Korea, Republic of, 102-752
- Recruiting
- Yonsei University Severance Hospital
-
Contact:
- Hyuk-Jae Chang, MD
- Phone Number: 82-2-2228-8454
- Email: hjchang@yuhs.ac
-
-
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
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
the siblings of premature coronary heart disease (male<55years old, female<65yeasrs old: Framingham Heart Study) patients admitted relevant hospital within 1 year
Description
Inclusion Criteria:
- within 1 year
- the siblings of premature coronary heart disease (male<55years old, female<65yeasrs old: Framingham Heart Study) patients admitted relevant hospital
Exclusion Criteria:
- Documented coronary heart disease
- experienced adverse events with relevant treatment
- contraindicated with beta-blockers
- Any woman of childbearing potential who is pregnant, seeking to become pregnant or suspects
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
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
evaluation of prevalence to coronary artery disease using CT
Time Frame: within 2 weeks from CT scanning
|
within 2 weeks from CT scanning
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Hyuk-Jae Chang, MD, PhD, Cardiology Division, Severance Cardiovascular Hospital, Yonsei University College of Medicine
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
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
June 1, 2009
Primary Completion (Anticipated)
September 1, 2012
Study Registration Dates
First Submitted
June 10, 2009
First Submitted That Met QC Criteria
June 10, 2009
First Posted (Estimate)
June 11, 2009
Study Record Updates
Last Update Posted (Estimate)
July 23, 2012
Last Update Submitted That Met QC Criteria
July 20, 2012
Last Verified
July 1, 2012
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 20090616
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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