Study of ADAMTS-13 Activity, Von Willebrand Factor and Platelet-Monocyte Aggregation in Coronary Artery Disease
NCT ID: NCT00905294
Last Updated: 2013-06-19
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.
TERMINATED
11 participants
OBSERVATIONAL
2009-08-31
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.
Platelet Function in Patients With an Acute Coronary Syndrome
NCT01992484
Measurement of Platelet Dense Granule Release in Healthy Volunteers
NCT00942617
Loss of Effect of Aspirin on Platelet Aggregation During Chronic Administration
NCT00748371
Aspirin in Patients With Myocardial Infarction and Thrombocytopenia
NCT00501345
Residual Platelet Activity Despite Aspirin Utilization in Coronary Heart Disease
NCT01820429
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
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
coronary artery disease
Subjects with coronary artery disease undergoing percutaneous coronary intervention
Blood draws
Observational: blood draws only
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Blood draws
Observational: blood draws only
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Planned percutaneous coronary intervention during admission
Exclusion Criteria
* Recent history (\< 6 months) of major surgery, trauma or thromboembolic event
* Percutaneous coronary or peripheral intervention or any stent placement performed within the past 6 months
* Current evidence of infection
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Royal College of Surgeons, Ireland
OTHER
University College Cork
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Professor Noel Caplice
Professor, Cardiovascular Sciences
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Noel M. Caplice, M.D, Ph.D.
Role: PRINCIPAL_INVESTIGATOR
University College Cork, Ireland
Dermot Kenny, M.D.
Role: STUDY_DIRECTOR
Royal College Surgeons in Ireland
David Foley, M.B.
Role: STUDY_DIRECTOR
Beaumont Hospital, Dublin, Ireland
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Cork University Hospital
Cork, , Ireland
Beaumont Hospital
Dublin, , Ireland
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.
INFACTs 2009-001
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.