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 @ 5:05 PM
Ignite Modification Date: 2025-12-24 @ 5:05 PM
NCT ID: NCT00906750
Eligibility Criteria: Inclusion Criteria: * Age 2 through 21 (not yet reached their 22nd birthday) at the time of entry into the study * Participant or participants parent/legal guardian available by telephone during the course of the study; * Written informed consent (and assent, if applicable) obtained * Currently receiving chemotherapy and /or radiotherapy for the treatment of cancer or have received chemotherapy in the past 12 weeks; * If the participant's underlying cancer is a solid tumor, current status must be stable disease, partial response, or complete response to therapy; if the participant's underlying disease is a hematological malignancy, current status must be in remission, and if receiving chemotherapy, must be in the "continuation" or "maintenance" phase of therapy or equivalent; * Estimated life expectancy of \> 1 year Exclusion Criteria: * History of hypersensitivity to any component of FluMist or TIV, including egg or egg products, gelatin, or monosodium glutamate; * History of hypersensitivity to gentamicin; * Close contact with a severely immunocompromised patient (e.g., a hematopoietic stem cell transplant patient, during those periods in which the immunocompromised patient requires care in a protective environment * History of Guillain-Barre“ syndrome; * History of asthma; * Female who is breastfeeding or lactating;
Healthy Volunteers: False
Sex: ALL
Minimum Age: 2 Years
Maximum Age: 21 Years
Study: NCT00906750
Study Brief:
Protocol Section: NCT00906750