- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00521326
Diagnosis and Characterization of Coronary Artery Stenosis by Doppler Ultrasound
August 24, 2007 updated by: Hillel Yaffe Medical Center
Diagnosis and Characterization of Coronary Artery Stenosis by Transthoracic Doppler Ultrasound
The purpose of this study is to evaluate the feasibility of acquisition of coronary blood flow velocity signals over the whole length of the LAD with transthoracic pulsed Doppler, and to evaluate the diagnostic power of the transthoracic Doppler analysis package for detecting and estimating the degree of coronary artery stenosis.
Finally we hope to optimize the currently available analysis package on the basis of the comparison of the Doppler with the angiographic stenosis results and evaluation.
Study Overview
Status
Unknown
Conditions
Study Type
Observational
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: Simcha R Meisel, MD, MSc
- Phone Number: 972-4-630-4656
- Email: meisel@hy.health.gov.il
Study Contact Backup
- Name: Avraham Shotan, MD
- Phone Number: 972-4-630-4428
- Email: shotana@yahoo.com
Study Locations
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Hadera, Israel, 38100
- Coronary Care Unit, Heart Institute, Hille Yaffe Medical Center
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Contact:
- Simcha R Meisel, MD, MSc
- Phone Number: 972-4-630-4656
- Email: meisel@hy.health.gov.il
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Principal Investigator:
- Simcha R Meisel, MD, MSc
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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
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
N/A
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Patients who are clinically suspected of having significant coronary artery stenosis.
- Patients with CAD.
- Patients who are scheduled to undergo coronary angiography.
- Signed informed consent.
Exclusion Criteria:
- Patients with arrhythmia / irregular pulse
- Patients with unstable conditions: unstable angina, uncontrolled CHF
- Patients with COPD
- Any physical or medical disability that prevent lying in supine position
- Patients with chest wall deformity
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: Defined Population
- Time Perspectives: Other
Cohorts and Interventions
Group / Cohort |
---|
A
Patients with an acute coronary syndrome that are candidates for coronary angiography.
Doppler results will be compared to angiographic findings.
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Simcha R Meisel, MD, MSc, Hillel Yaffe 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
August 1, 2007
Study Registration Dates
First Submitted
August 24, 2007
First Submitted That Met QC Criteria
August 24, 2007
First Posted (Estimate)
August 27, 2007
Study Record Updates
Last Update Posted (Estimate)
August 27, 2007
Last Update Submitted That Met QC Criteria
August 24, 2007
Last Verified
March 1, 2007
More Information
Terms related to this study
Keywords
- coronary stenosis
- doppler
- non-invasive testing
- A prospective study of a new diagnostic method.
- Study consists of a transthoracic doppler of LAD.
- Doppler to be performed prior to coronary angiography.
- F/U doppler examination for those who undergo PCI.
- Doppler results will be compared with coronary angiography.
Additional Relevant MeSH Terms
Other Study ID Numbers
- DOP01
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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