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 @ 3:31 AM
Ignite Modification Date:
2025-12-25 @ 3:31 AM
NCT ID:
NCT03448705
Eligibility Criteria:
Inclusion Criteria:
* Adult persons aged 18 to 59 years, determined on the day of enrolment from both sexes, mentally competent;
* Good health (as determined by vital signs and existing medical condition) or stable medical condition. Subjects will not be excluded with known adequately treated clinically significant organ or systemic diseases (e.g. asthma or insulin treated), the significance of which, in the opinion of the investigator, will not compromise the subject's participation in the study;
* Female volunteers of childbearing potential upon the decision of the investigator with a negative result from the urine pregnancy test prior to vaccination who agrees to use an acceptable contraception method or abstinence throughout the trial and to not become pregnant for the duration of the study;
* Capability of participants to understand and comply with planned study procedures;
* Participants provide written informed consent prior to initiation of study procedures;
* Absence of any exclusion criteria.
Exclusion Criteria:
* Pregnancy, breast feeding or positive urine pregnancy test at baseline prior to vaccination. Female subjects who are able to bear children but not willing to use an acceptable contraception method for the duration of the study. Pregnancy with regard to the total duration of the study.
* Hypersensitivity to the active substances or to any of the excipients, such as thiomersal, or any component that may be present in traces, such as egg (ovalbumin), formaldehyde, gentamicin, neomycin, vancomycin or ciprofloxacin determined prior to vaccination;
* Serious complications in the medical history with regard to any previous vaccination: encephalitis/encephalopathy, nonfebrile seizures, Guillain-Barré syndrome, vasculitis, neuritis, facial paresis determined prior to vaccination;
* History of neurological symptoms or signs, or anaphylactic shock following administration of any vaccine determined prior to vaccination;
* Serious disease, such as cancer, autoimmune disease, advanced arteriosclerotic disease, complicated diabetes mellitus, acute or progressive hepatic disease, acute or progressive renal disease, congestive heart failure with regard to the total duration of the study;
* Immunosuppressive therapy within 36 months prior to vaccination and with regard to the total duration of the study;
* Concomitant corticosteroid therapy, including high-dose inhaled corticosteroids with regard to the total duration of the study;
* Receipt of immunostimulants with regard to the total duration of the study;
* Receipt of parenteral immunoglobulin, blood products and/or plasma derivate within 3 months prior to vaccination and with regard to the total duration of the study;
* Suspected or known HIV, Hepatitis-B virus (HBV) or Hepatitis-C virus (HCV) infection with regard to the total duration of the study;
* Acute disease and/or axillary temperature ≥37oC within 3 days prior to vaccination;
* Vaccine therapy within 4 weeks prior to vaccination and with regard to the total duration of the study;
* Influenza vaccination (any kind) within 6 months prior to vaccination and with regard to the total duration of the study;
* Experimental drug therapy within 4 weeks prior to vaccination and with regard to the total duration of the study;
* Concomitant participation in another clinical study;
* Any condition which, may interfere with the evaluation of the study (including major protocol deviation with regard to the total duration of the study);
* Past or current psychiatric disease of the volunteer that upon judgement of the investigator may have an effect on the objective decision-making of the volunteer;
* Alcohol or drug abuse of the participant.
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
59 Years
Study:
NCT03448705
Study Brief:
Protocol Section:
NCT03448705