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 @ 1:00 PM
Ignite Modification Date:
2025-12-24 @ 1:00 PM
NCT ID:
NCT04235361
Eligibility Criteria:
Inclusion criteria
* All subjects (male, female, adults and children) meeting the WHO case definition of "suspected" and "probable" EVD case eligible for real time RT-PCR assay, according to the currently used case definition in DRC.
* For the prospective evaluation, oral informed consent from the patient/legal guardian will be requested for eligibility to participate in the study
Exclusion criteria:
* inability to provide consent, samples or condition that could jeopardize the subject's safety.
Healthy Volunteers:
False
Sex:
ALL
Study:
NCT04235361
Study Brief:
Protocol Section:
NCT04235361