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 @ 5:57 PM
Ignite Modification Date: 2025-12-24 @ 5:57 PM
NCT ID: NCT04051268
Eligibility Criteria: Inclusion Criteria: * Healthy. * Subject/Parents/legal guardian(s) have been informed properly regarding the study and signed the informed consent form/and informed assent form. * Subject/parents/legal guardian(s) will commit to comply with the instructions of the investigator and the schedule of the trial. Exclusion Criteria: * Subject concomitantly enrolled or scheduled to be enrolled in another trial. * Evolving mild, moderate or severe illness, especially infectious diseases or fever (axilary temperature ³ 37.5°C). * Known history of allergy to any component of the vaccines. * History of uncontrolled coagulopathy or blood disorders contraindicating intramuscular injection. * Subject who has received in the previous 4 weeks a treatment likely to alter the immune response (intravenous immunoglobulins, blood-derived products, corticosteroid therapy and other immunosuppressants) * Any abnormality or chronic disease which according to the investigator might interfere with the assessment of the trial objectives. * Pregnancy \& lactation (Adults). * Individuals who have previously received any vaccines against typhoid fever. * Subjects already vaccinated with any vaccine within one month prior and expect to receive other vaccines within one month following vaccination except MR (Measles Rubella) vaccine. * Individuals who have a previously ascertained typhoid fever by laboratory confirmation (blood culture/new rapid test) at any time. * Subject planning to move from the study area before the end of study period.
Healthy Volunteers: True
Sex: ALL
Minimum Age: 6 Months
Maximum Age: 60 Years
Study: NCT04051268
Study Brief:
Protocol Section: NCT04051268