Clinical Trials Directory

Trials / Completed

CompletedNCT00728286

Assessment of Thrombogenicity in Acute Coronary Syndrome

Assessment of Platelet-dependent Thrombosis in Patients With Acute Coronary Syndromes Using an ex Vivo Arterial Injury Model

Status
Completed
Phase
Study type
Observational
Enrollment
90 (actual)
Sponsor
Newcastle-upon-Tyne Hospitals NHS Trust · Academic / Other
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to assess platelet dependent thrombogenicity in patients after acute coronary syndrome using an ex vivo arterial injury model.

Detailed description

Abnormal platelet activity seen in patients with Type2 Diabetes Mellitus (T2DM) may be an important contributor to their enhanced cardiovascular risk and higher rates of cardiovascular events following acute coronary syndrome, despite dual antiplatelet therapy with aspirin and clopidogrel. We have earlier demonstrated high thrombogenicity in individuals with T2DM and CAD in the absence of acute ischaemic events, despite therapeutic doses of aspirin.We hypothesise that patients with T2DM will have increased thrombogenicity after acute coronary syndrome despite optimal secondary prevention medication.Measuring ex vivo thrombus area using an arterial injury model simulates plaque rupture and reflects the summative effect of all haemostatic abnormalities. The thrombus area of patients with ACS and T2DM will be compared to the controls without T2DM.

Conditions

Timeline

Start date
2008-10-01
Primary completion
2011-01-01
Completion
2011-05-01
First posted
2008-08-05
Last updated
2015-10-12

Locations

1 site across 1 country: United Kingdom

Source: ClinicalTrials.gov record NCT00728286. Inclusion in this directory is not an endorsement.