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 @ 1:38 AM
Ignite Modification Date:
2025-12-25 @ 1:38 AM
NCT ID:
NCT01626794
Eligibility Criteria:
Inclusion Criteria:
* negative clinical history of measles, mumps, rubella, varicella, and zoster
Exclusion Criteria:
* received any measles, mumps, rubella, or varicella vaccine at any time prior to the study, or is anticipated to receive any of these vaccines outside the study
* any congenital or acquired immune deficiency, neoplastic disease, or depressed immunity
* received systemic immunomodulatory steroids within 3 months prior to entering the study or is expected to require them throughout the study
* history of allergy or anaphylactoid reaction to neomycin, gelatin, sorbital, egg proteins, chicken proteins, or any components of M-M-R™ II or VARIVAX™
* received salicylates within 14 days prior to study vaccination
* exposed to measles, mumps, rubella, varicella, or zoster in the 4 weeks prior to study vaccination
* received any non-live vaccine within 14 days prior to any study vaccination or is expected to received such vaccine during the 42-day period after each study vaccination
* received any live vaccine within 30 days prior to any study vaccination or is expected to received such vaccine during the 42-day period after each study vaccination
* received immune globulin, a blood transfusion, or blood-derived products within 5 months prior to any study vaccination
* fever illness (≥102.2°F \[39.0°C\]) within 72 hours prior to study vaccination
* born to a human immunodeficiency virus (HIV)-infected mother
* participated in any other clinical trial (other than a surveillance study) within 30 days prior to study enrollment
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
12 Months
Maximum Age:
23 Months
Study:
NCT01626794
Study Brief:
Protocol Section:
NCT01626794