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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT00905294
Other study ID # INFACTs 2009-001
Secondary ID
Status Terminated
Phase N/A
First received May 19, 2009
Last updated June 17, 2013
Start date August 2009
Est. completion date August 2010

Study information

Verified date June 2013
Source University College Cork
Contact n/a
Is FDA regulated No
Health authority Ireland: Medical Ethics Research Committee
Study type Observational

Clinical Trial Summary

The purpose of this research is to determine the relationship between proteins and enzymes in the blood and how they work with platelets to form blood clots in patients with coronary artery disease. The investigators hypothesize that the relationship between these factors could potentially be useful in identifying patients at higher risk for heart attacks.


Recruitment information / eligibility

Status Terminated
Enrollment 11
Est. completion date August 2010
Est. primary completion date August 2010
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Admission to hospital with suspected index event of Non-ST-Elevation Myocardial Infarction (NSTEMI), Unstable Angina (UA) or Stable Angina (SA)

- Planned percutaneous coronary intervention during admission

Exclusion Criteria:

- Recent history (< 6 months) of an acute coronary syndrome (other than current admission) or stroke

- 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

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Intervention

Other:
Blood draws
Observational: blood draws only

Locations

Country Name City State
Ireland Cork University Hospital Cork
Ireland Beaumont Hospital Dublin

Sponsors (2)

Lead Sponsor Collaborator
University College Cork Royal College of Surgeons, Ireland

Country where clinical trial is conducted

Ireland, 

Outcome

Type Measure Description Time frame Safety issue
Primary relationships between ADAMTS-13 activity, von Willebrand factor antigen and platelet-monocyte aggregates levels Assess the relationships between ADAMTS-13 activity, von Willebrand factor antigen and platelet-monocyte aggregates levels in subjects with coronary artery disease prior to and after undergoing PCI in this exploratory study change from baseline to after percutaneous coronary intervention No
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