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 @ 1:02 AM
Ignite Modification Date:
2025-12-25 @ 1:02 AM
NCT ID:
NCT06509893
Eligibility Criteria:
Inclusion Criteria:
* Male or female above 20 years of age undergoing PCI with a drug-eluting stent for chronic coronary syndrome
* The patient has provided written informed consent as approved by the ethics committee of the Shiraz University of Medical Sciences.
Exclusion Criteria:
* Contraindication to aspirin, clopidogrel, ticagrelor, or any other reason that study drug should not be administered (including hypersensitivity, moderate or severe liver disease, active bleeding, and major surgery within 30 days)
* Atrial fibrillation or other indication for oral anticoagulant therapy.
* Concomitant oral or IV therapy with strong CYP3A inhibitors, CYP3A substrates with narrow therapeutic indices (cyclosporine, and quinidine), or strong CYP3A inducers ( rifampin, rifampicin, phenytoin, and carbamazepine)
* Females of child-bearing age unless negative pregnancy test at screening and willing to use effective contraception for the duration of trial
* Females who are breastfeeding at the time of enrolment.
* Unsuccessful PCI or PCI without optimal stent placement; this decision is made by the supervising interventional cardiologist.
* patients with anatomical SYNTAX score ≥23 prior to PCI
* Patients with planned surgical intervention to treat any cardiac or non-cardiac condition.
* Previous PCI in the last 6 months.
* Current (same hospitalization) or previous (within 12 months) acute coronary syndrome.
* History of definite stent thrombosis.
* Concomitant cardiac valve disease requiring invasive therapy.
* Acute heart failure.
* Active myocarditis.
* Cardiomyopathy.
* Patient in hemodialysis.
* History of stroke or transient ischemic cerebrovascular accident.
* History of intracranial hemorrhage or other intracranial pathology associated with increased bleeding risk.
* Hemoglobin \<10 g/dL
* Peptic ulceration documented by endoscopy within the last 3 months unless healing proven by repeat endoscopy.
* Any other condition deemed by the investigator to place the patient at excessive risk of bleeding with ticagrelor.
* Participation in another trial with an investigational drug or device.
* Assessment that the subject is not likely to comply with the study procedures or have complete follow-up.
* Known drug or alcohol dependence within the past 12 months as judged by the investigator.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
20 Years
Maximum Age:
80 Years
Study:
NCT06509893
Study Brief:
Protocol Section:
NCT06509893