The Project: Every Child Protocol: A Registry Eligibility Screening Biology and Outcome Study
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- STATUS
- Recruiting
Summary
This research trial studies the Project: Every Child for younger patients with cancer. Gathering health information over time from younger patients with cancer may help doctors find better methods of treatment and on-going care.
Description
The purpose of this study is to maintain a Childhood Cancer Registry for infants, children, adolescents, and young adults with cancer; to utilize clinical and biological data to help determine eligibility or stratification, based on childhood cancer disease classification schemas, for potential enrollment of research subjects onto Children's Oncology Group (COG) therapeutic clinical trials; to develop a well annotated childhood cancer biobank for current and future research through the collection of biospecimens (at diagnosis, time of progression, time of recurrence and/or post-mortem), including tumor, host and when feasible parental germline deoxyribonucleic acid (DNA); and key clinical data, including presentation, diagnostic, staging, summary treatment, and outcome information, from every child diagnosed with cancer at COG institutions; and to allow use of registry data for permission to be contacted in the future to consider participating in non-therapeutic and prevention research studies involving the child or their parents.
FAQ
Details
| Condition | Childhood Lymphoma,Childhood Relapsed Solid Tumor,Central Nervous System Neoplasm,lymphoma,neoplasm,childhood,child,children,kid,kids,teen,teens,teenager,teenagers,pediatric,riley,registry,database,solid tumor,relapsed,refractory,cancer,oncology |
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| Age | 25years or below |
| Clinical Study Identifier | TX6425 |
| Last Modified on | 19 February 2024 |
Eligibility
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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.
Learn moreIf you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.
Learn moreComplete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.
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