Carotid Intraplaque Neovascularization Combined With Stress Echo
NCT ID: NCT05416385
Last Updated: 2025-02-06
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
RECRUITING
1500 participants
OBSERVATIONAL
2021-08-16
2026-08-16
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Intracoronary Imaging With NIRS-IVUS to Characterize Arterial Plaques
NCT01694368
Intracoronary Features in the Prognosis of Endothelial Dysfunction and MACES in Population With Acute Coronary Syndrome
NCT03583047
Correlation Between Coronary and Carotid Atherosclerotic Disease (CAD) and Links With Clinical Outcomes
NCT01353612
Optical Coherence Tomography to Improve Clinical Outcomes During Coronary Angioplasty
NCT02065102
Does OCT Imaging Allow us to See Blood Vessel Development in and Around Deposits of Fat and Calcium Inside Blood Vessels
NCT03182348
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Objectives: 1) The % change in test sensitivity of IPN+SE for predicting 3-year MACE compared with SE alone. 2) The Net Reclassification Improvement (NRI) for MACE will be determined (patients "missed" by the SE, but captured as high risk for MACE by IPN).
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Cardiac outpatients
Subjects referred for outpatient stress echocardiogram (SE).
Carotid Contrast Enhanced Ultrasound
Carotid Contrast-Enhanced Ultrasound (CEUS), a diagnostic ultrasound enhancing agent that opacifies the blood to delineate the vessel walls.
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Carotid Contrast Enhanced Ultrasound
Carotid Contrast-Enhanced Ultrasound (CEUS), a diagnostic ultrasound enhancing agent that opacifies the blood to delineate the vessel walls.
Other Intervention Names
Discover alternative or legacy names that may be used to describe the listed interventions across different sources.
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
2. Referred for a clinically indicated SE for assessment of ischemia and risk stratification;
3. Able and willing to give informed consent.
Exclusion Criteria
2. Referral for viability, pulmonary hypertension, or valve assessment;
3. Referral outside of the normal working hours;
4. History of significant CAD: percutaneous coronary intervention (PCI), coronary artery bypass graft (GABG), or coronary angioplasty;
5. History of stroke or myocardial infarction (MI);
6. Known or documented hypersensitivity or allergy to perflutren (DEFINITY® contrast agent);
7. Known or documented allergy to Polyethylene Glycol (Peg) a component of DEFINITY®;
8. History of carotid surgery (endarterectomy or stenting);
9. Any serious medical condition or complication from the stress test that according to the investigator could interfere with the carotid scan or optimal care;
10. Currently pregnant or breastfeeding;
11. Previous enrolment into the study.
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Lantheus Medical Imaging
INDUSTRY
Dr. Amer Johri
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Dr. Amer Johri
Professor
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Amer Johri, MD
Role: PRINCIPAL_INVESTIGATOR
Queen's University
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
University of Calgary
Calgary, Alberta, Canada
University of Alberta
Edmonton, Alberta, Canada
Dalhousie University
Halifax, Nova Scotia, Canada
The Kingston Heart Clinic
Kingston, Ontario, Canada
Queen's University, Cardiovascular Imaging Network at Queen's (CINQ)
Kingston, Ontario, Canada
Unity Health Toronto
Toronto, Ontario, Canada
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
CG#21007
Identifier Type: OTHER_GRANT
Identifier Source: secondary_id
452696
Identifier Type: OTHER
Identifier Source: secondary_id
DMED-2469-21-6032717
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.