A Randomized Trial of Clinical Decision Making in Asymptomatic Carotid Stenosis
NCT ID: NCT01315288
Last Updated: 2024-01-05
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.
COMPLETED
NA
409 participants
INTERVENTIONAL
2008-10-31
2010-08-31
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.
Innovative Application of Pressure Gradient Measurement in Internal Carotid Stenosis in Patients Undergoing CAS
NCT06123767
Carotid Asymptomatic Stenosis
NCT04825080
Assessment of Cognitive Function in Patients Undergoing Carotid Artery Stent Placement
NCT00919165
Impact of Aspiration Thrombectomy During Carotid Stenting
NCT01550835
Noninvasive Evaluation for Carotid Artery Stenosis: The Carotid Stenotic Scan
NCT04057183
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
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.
RANDOMIZED
PARALLEL
PREVENTION
QUADRUPLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Video presentation absolute risk
absolute risk
One of 6 video presentation by one of 4 presenters
Video presentation absolute event-free survival
absolute event-free survival
One of 6 video presentation by one of 4 presenters
Video presentation annualized absolute risk
annualized absolute risk
One of 6 video presentation by one of 4 presenters
Video presentation relative risk
relative risk
One of 6 video presentation by one of 4 presenters
Video presentation qualitative description
qualitative description
One of 6 video presentation by one of 4 presenters
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
One of 6 video presentation by one of 4 presenters
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
Exclusion Criteria
* Unable to read English
18 Years
ALL
Yes
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Henry Ford Health System
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Henry Ford Hospital
Detroit, Michigan, United States
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
ACSCDM-1
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.