- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06253962
Carotid Atherosclerosis in Predicting Coronary Artery Disease (CACA)
February 4, 2024 updated by: Shanghai Zhongshan Hospital
Carotid plaque burden and composition features, particularly lipid necrotic core, are significantly associated with severity of CAD stenosis.
This study aims to explore the relationship between various phenotypic patterns of carotid atherosclerosis with the prevalence, phenotype, and severity of coronary atherosclerosis.
The patients with chest tightness or chest pain will receive carotid artery ultrasonography before coronary angiography so as to explore the relationship between them.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Estimated)
1000
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: Danbo Lu, PhD
- Phone Number: +86 021 64041990
- Email: lu.danbo@zs-hospital.sh.cn
Study Locations
-
-
-
Shanghai, China, 200032
- Recruiting
- 180 Fenglin Road
-
Contact:
- Danbo Lu, PhD
- Phone Number: +86 021 64041990
- Email: lu.danbo@zs-hospital.sh.cn
-
-
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
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
Patients admitted to receive coronary angiography.
Carotid ultrasound performed before angiography.
Description
Inclusion Criteria:
- patients receive carotid ultrasound and coronary angiography
Exclusion Criteria:
- None
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
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
carotid atherosclerosis
|
severity of coronary atherosclerosis
|
without carotid atherosclerosis
|
severity of coronary atherosclerosis
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
MACE
Time Frame: two years after angiography
|
acute myocardial infarction; heart failure; cardiac death; revascularization
|
two years after angiography
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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 (Estimated)
February 10, 2024
Primary Completion (Estimated)
December 31, 2026
Study Completion (Estimated)
December 31, 2028
Study Registration Dates
First Submitted
February 4, 2024
First Submitted That Met QC Criteria
February 4, 2024
First Posted (Actual)
February 12, 2024
Study Record Updates
Last Update Posted (Actual)
February 12, 2024
Last Update Submitted That Met QC Criteria
February 4, 2024
Last Verified
February 1, 2024
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- CACA
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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