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 @ 11:14 PM
Ignite Modification Date:
2025-12-24 @ 11:14 PM
NCT ID:
NCT01807169
Eligibility Criteria:
Inclusion Criteria:
* Age ≥ 18 years, male or female
* Polypectomy AND / OR mucosectomy (EMR) performed on clopidogrel and/or aspirin during a colonoscopy with inability to defer action
* Taking a single daily dose of clopidogrel long-term (more than 3 months) or under treatment with clopidogrel and aspirin (aspirin \< 375 mg more than 3 months) in the prevention of cardiovascular and thromboembolic risk with a major or medium - secondary prevention
* Affiliation to the regime of national health protection
* Informed consent and patient's written obtained
* No participation in another clinical study
Exclusion Criteria:
* Contraindications to the achievement of a lower gastrointestinal endoscopy
* Taking a single daily dose of clopidogrel or other anti-platelet, anti vitamin K (AVK), heparin or anti bi aggregation in the context of cardiovascular prevention
* Taking chronic anti inflammatory drug (at least once weekly)
* Resection technique submucosal dissection
* Haemorrhagic disease, disorders of hemostasis and coagulation (PT \<60%, aPTT\> 40 sec. And platelets \<100000/mm3), hematologic malignancy, chronic liver cirrhosis classified as Child Pugh B or C, acute or chronic renal failure
* Acute Coronary Syndrome \<3 months or not received percutaneous coronary intervention (PCI).
* Angioplasty with placement of a stent drug evaluation (out of context of acute coronary syndrome) \<3 months.
* Angioplasty with placement of a bare metal stent (out of context of acute coronary syndrome) \<4 weeks.
* Pregnant women, nursing
* Not signing the written consent and / or mental disabilities of the subject making its participation in the trial impossible
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT01807169
Study Brief:
Protocol Section:
NCT01807169