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: 2025-12-24 @ 10:45 PM
Ignite Modification Date: 2025-12-24 @ 10:45 PM
NCT ID: NCT04327635
Eligibility Criteria: Inclusion Criteria: * Undergoing ≥1 elective, urgent, or emergent coronary stent implantation * Angiographic evidence of TIMI 3 flow through the stented vessel after stent placement * Angiographic evidence of residual stenosis visually \<30% after stent placement * Willing and able to provide signed informed consent * Lives within 90 mile radius of study site * Willing and able to return to study site for all follow-up visits Exclusion Criteria: * Prior solid organ transplantation at any time * Pregnant or lactating at screening * Known presence of chronic systemic inflammatory disorder that requires ongoing therapy with immunosuppressive agents * Known immune system compromise including but not limited to human immunodeficiency virus (HIV), hepatitis A, hepatitis B (HBV) or hepatitis C (HCV) infection * Known history of malignancy of any type except non-melanoma skin cancer * Known serum creatinine \>2 mg/dL or GFR ≤30 mL/min within the last twelve months * Known AST, ALT, and/or bilirubin (total) elevated twice the upper limit of normal for age \& gender within the last twelve months * Known Hemoglobin lower than 8.0 g/dL within the last twelve months * Known current illicit drug use at screening * Other major surgical procedure or major trauma within the previous 14 days prior to enrollment * Female of child bearing potential who is unwilling to agree to use acceptable contraception methods for 3 months after receiving the investigational drug * Pacemaker/ICD implant in place * Adult lacking decision-making capacity * Prisoner * Non-English speaking * English-speaking but illiterate * Legally blind * Known allergy to heparin or heparin-induced thrombocytopenia * Known history of positive SARS-CoV2 testing within the last 30 days * DNR/DNI status prior to PCI procedure or planned DNR/DNI status after PCI procedure * Homeless or no permanent address at the time of enrollment
Healthy Volunteers: False
Sex: ALL
Minimum Age: 21 Years
Maximum Age: 85 Years
Study: NCT04327635
Study Brief:
Protocol Section: NCT04327635