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 @ 1:32 AM
Ignite Modification Date:
2025-12-25 @ 1:32 AM
NCT ID:
NCT00584194
Eligibility Criteria:
Inclusion Criteria:
Parts A \& B:
* At least 18 years old, or if active military duty, 17 years old,
* Females of childbearing potential must agree to have a urine pregnancy test within 48 hours before receipt of each dose of vaccine. The test results must be negative. Females will be advised not to become pregnant for 3 months after the primary series and each booster dose, and must not be breast-feeding,
* Subject must be actively enrolled in the SIP to be vaccinated at USAMRIID or be otherwise authorized (with documentation) by the DOD
* Subjects must be at risk for exposure to RVF virus,
* Subjects must have an up-to-date (within 1 year) medical history, physical examination, and laboratory tests in their charts and be medically cleared for participation by an investigator. Examinations or tests may be repeated within 1 year at the discretion of the enrolling physician.
* Volunteer must have signed and dated the approved informed consent (Volunteer Agreement Explanation and Affidavit).
Additional Inclusion Criteria for Part B:
• Completion of primary series and any follow-up titer (PRNT80) \< 1:40 from the current or a previous RVF IND 365 protocol.
Exclusion Criteria
Parts A \& B:
* Clinically significant abnormal lab results including evidence of Hepatitis C, Hepatitis B or carrier state, or elevated liver function tests.
* Personal history of immunodeficiency or current treatment with immunosuppressive medication, at the discretion of the physician.
* Confirmed HIV infection.
* Any medical condition that, at the discretion of the physician, may jeopardize the safety of the volunteer.
* Any serious or life-threatening allergies to any component of the vaccine: formalin, human serum albumin, neomycin, streptomycin
* Administration of any other vaccine within 28 days of any dose of RVF vaccine.
* Any unresolved adverse event resulting from a previous immunization.
Additional Exclusion Criteria for Part B:
• An adequate PRNT80 (≥ 1:40) after completion of primary series.
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
17 Years
Study:
NCT00584194
Study Brief:
Protocol Section:
NCT00584194