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
109 participants
OBSERVATIONAL
2021-06-17
2021-06-29
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
This is a retrospective study with patients who underwent primary PCI for STEMI between March 2020 to May 2021. The primary outcome of this study is the access-site complication including major bleeding requiring transfusion or surgery, hematoma and arterial occlusion.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Comparison of Success Rate Between Distal Radial Approach and Radial Approach in STEMI
NCT03611725
Distal Transradial Access for Primary Percutaneous Coronary Intervention in STEMI Patients
NCT04861389
Distal Versus Conventional Transradial Artery Access for Coronary Catheterization in Patients With STEMI
NCT05605288
Randomized Comparison of Distal Radial Versus Conventional Radial Access for Coronary Angiography and Intervention
NCT04784078
Distal Radial Access for Primary PCI in STEMI Patients to Prevent RAO
NCT05461781
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.
COHORT
RETROSPECTIVE
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Distal radial access
Vascular access for primary PCI in patients with STEMI
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
Exclusion Criteria
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Yonsei University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Yongcheol Kim
Professor
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Yongcheol Kim
Role: PRINCIPAL_INVESTIGATOR
Yongin Severance Hopistal
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Yongin Severance Hospital
Yongin, Gyeonggi-do, South Korea
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.
DRA-STEMI
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.