Eligibility Module

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: 2025-12-25 @ 4:27 AM
Ignite Modification Date: 2025-12-25 @ 4:27 AM
NCT ID: NCT01476020
Eligibility Criteria: Inclusion Criteria: * Male or female subject ≥ 18 years of age eligible for PCI with at least one drug eluting stent (name: Xience) implanted in all clinical situations excluding primary PCI for acute MI and treatment of the left main artery. * Male or female subject ≥ 18 years of age eligible for PCI with at least one DES Xience. * Patient not pre-treated with protein IIb/IIIa inhibitors (name: abxicimab or eptifibatide) during hospitalization * Patient pre-treated with aspirin and clopidogrel before PCI * ASA check at least 24 hours after the interruption of tirofiban * The subject has given written informed and dated consent to participate in this study. Exclusion Criteria: * Subjects not able to give informed consent * Prior implantation of DES * Known platelets \< 100 000/µl or known hemorrhagic diathesis * Oral anticoagulation or treatment with abxicimab or eptifibatide during hospitalization * ASA check less than 24 hours after the interruption of tirofiban * Thrombolytic therapy within 4 days before ASA check * Contra-indication to aspirin or clopidogrel * Recent major surgery \< 6 weeks * Evidence of an active gastrointestinal or urogenital bleeding * Severe liver insufficiency * Primary PCI for acute MI * Left main PCI * Any scheduled surgery during the year after enrollment * Severe concomitant disease with life expectation \< two years
Healthy Volunteers: False
Sex: ALL
Minimum Age: 18 Years
Study: NCT01476020
Study Brief:
Protocol Section: NCT01476020