Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 5:37 PM
Ignite Modification Date:
2025-12-24 @ 5:37 PM
NCT ID:
NCT00914368
Eligibility Criteria:
Inclusion Criteria:
* Provide signed written informed consent.
* Male or female patients above 18 years old.
* Previous PCI and coronary stenting for coronary artery disease
* Previous (after coronary stenting) or current dual antiplatelet treatment (aspirin 75 mg once daily (o.d) and clopidogrel 75 mg o.d). All patients need to be on treatment with aspirin 75 mg once daily at least seven days prior to enrollment.
* Experienced one of the following alternatives:
* Stent thrombosis within 6 months of PCI while on dual antiplatelet treatment; OR
* Experienced MI within 6 month after coronary stenting while on dual antiplatelet treatment; OR
* No experience of stent thrombosis or MI for at least 6 months and until visit 1 (matched control)
Exclusion Criteria:
General exclusion criteria:
1. Women who are known to be pregnant, who have given birth within the past 90 days, or who are breastfeeding.
2. Any condition or laboratory findings which in the opinion of the Investigator makes the patient unsuitable for inclusion
3. Enrolled in either another investigational drug study or in another investigational study of an approved drug within 30 days prior to Visit 1 of the current study.
4. Known allergies or intolerance to aspirin and/or thienopyridines (clopidogrel or ticlopidine).
5. Significant active neuropsychiatric disease, alcohol abuse or drug abuse, in the investigator's opinion.
6. UCR or Accumetrics employees or investigator site personnel directly affiliated with this study, and their immediate families. Immediate family is defined as a spouse, parent, child or sibling, whether biological or legally adopted.
Cardiovascular Exclusion Criteria:
7. Subjects with unstable coronary artery disease, defined as new, increased, or rest angina at screening.
8. Subjects with significant hypertension (systolic blood pressure \> 180 mm Hg or diastolic blood pressure \>110 mmHg) at the time of screening.
Bleeding Risk Exclusion Criteria:
9. Any known contraindication to treatment with an anticoagulant or antiplatelet agent.
10. Prior history or presence of significant bleeding disorders (for example,hematemesis, melena, severe or recurrent epistaxis, hemoptysis, hematuria, or intraocular bleeding)
11. Prior history or clinical suspicion of cerebral vascular malformations
12. Prior history of abnormal bleeding tendency (i.e. prolonged bleeding on dental extraction, tonsillectomy, or previous surgical procedure).
13. Personal or family history of coagulation or bleeding disorders.
14. Thrombocytopenia (platelet count \< 100,000/mm3) or thrombocytosis (platelet count \> 500,000/mm3).
15. History of major surgery, severe trauma, organ biopsy within 3 months prior to enrollment.
16. Any planned surgical procedure within 20 days following inclusion.
17. The use (or planned use) of other antiplatelet agents (besides aspirin and clopidogrel), anticoagulant or fibrinolytic agents.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT00914368
Study Brief:
Protocol Section:
NCT00914368