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 @ 2:01 AM
Ignite Modification Date: 2025-12-25 @ 2:01 AM
NCT ID: NCT03147560
Eligibility Criteria: Inclusion Criteria: * Parent/legal acceptable representative is willing and able to understand the protocol requirements and provide informed consent. * Participant is aged ≥ 60 days to ≤ 75 days. * Participant without preventive inoculation of polio vaccine and previous history of Polio. * Subject and parent/guardian able to attend all scheduled visits and comply with all trial procedures. * Body temperature ≤ 37.5℃. Exclusion Criteria: * Known allergy to any constituent of the vaccine. * Known acute illness, severe chronic disease, acute exacerbation of chronic disease and fever. * Known or suspected impairment of immunologic function, or receipt of immunosuppressive therapy or immunoglobulin since birth. * Reported the history of allergies, convulsions, epilepsy, mental illness and brain disease and clear serious systemic reaction. * Known bleeding disorder. * Receipt of the whole blood, blood plasma or immunoglobulin before the trial vaccination. * Reported the history of acute illness had need systemic antibiotics or antiviral treatment of infections in the 7 days preceding the trial vaccination. * An acute illness with or without fever (temperature ≥ 38.0℃) in the 3 days preceding enrollment in the trial. * Participation in any other intervention clinical trial. * Any condition which, in the opinion of the investigator, would pose a health risk to the subject or interfere with the vaccine.
Healthy Volunteers: False
Sex: ALL
Minimum Age: 60 Days
Maximum Age: 75 Days
Study: NCT03147560
Study Brief:
Protocol Section: NCT03147560