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Trial details imported from ClinicalTrials.gov
For full trial details, please see the original record at
https://clinicaltrials.gov/study/NCT02402244
Registration number
NCT02402244
Ethics application status
Date submitted
25/03/2015
Date registered
30/03/2015
Date last updated
25/07/2024
Titles & IDs
Public title
Project: Every Child for Younger Patients With Cancer
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Scientific title
The Project: EveryChild Protocol: A Registry, Eligibility Screening, Biology and Outcome Study
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Secondary ID [1]
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NCI-2014-02057
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Secondary ID [2]
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APEC14B1
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Adrenal Gland Pheochromocytoma
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Carcinoma In Situ
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Central Nervous System Neoplasm
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Childhood Immature Teratoma
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Childhood Langerhans Cell Histiocytosis
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Childhood Mature Teratoma
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Congenital Mesoblastic Nephroma
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Desmoid Fibromatosis
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Ganglioneuroma
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Lymphoproliferative Disorder
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Malignant Neoplasm
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Malignant Solid Neoplasm
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Melanocytic Neoplasm
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Myeloproliferative Neoplasm
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Neoplasm of Uncertain Malignant Potential
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Neuroendocrine Neoplasm
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Stromal Neoplasm
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Condition category
Condition code
Cancer
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Cervical (cervix)
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Cancer
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Breast
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Cancer
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Neuroendocrine tumour (NET)
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Cancer
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Other cancer types
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Cancer
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Brain
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Cancer
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Children's - Brain
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Renal and Urogenital
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Other renal and urogenital disorders
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Cancer
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Malignant melanoma
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Respiratory
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Other respiratory disorders / diseases
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Cardiovascular
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Diseases of the vasculature and circulation including the lymphatic system
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Cancer
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Leukaemia - Acute leukaemia
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Cancer
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Leukaemia - Chronic leukaemia
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Cardiovascular
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Diseases of the vasculature and circulation including the lymphatic system
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Inflammatory and Immune System
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Other inflammatory or immune system disorders
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Intervention/exposure
Study type
Observational
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Patient registry
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Target follow-up duration
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Target follow-up type
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Description of intervention(s) / exposure
Other interventions - Cytology Specimen Collection Procedure
Other interventions - Medical Chart Review
Observational (Project: Every Child) - Patients undergo medical data review to create a Childhood Cancer Registry. Patients also undergo collection of biospecimen samples (e.g., tissue, blood, bone marrow, plasma, serum, buccal swab, saliva, cerebrospinal fluid, or urine).
Other interventions: Cytology Specimen Collection Procedure
Undergo cytology specimen collection
Other interventions: Medical Chart Review
Undergo medical data review
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Intervention code [1]
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Other interventions
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Comparator / control treatment
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Control group
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Outcomes
Primary outcome [1]
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Number of patients who consented to biobanking
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Assessment method [1]
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The number of patients who agree to be in the Biobanking part of the study and have leftover tumor tissue and some normal blood, bone marrow, or other tissue saved for future research.
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Timepoint [1]
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Baseline
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Eligibility
Key inclusion criteria
* Enrollment must occur within 6 months of initial disease presentation OR within 6 months of refractory disease, disease progression, disease recurrence, second or secondary malignancy, or post-mortem
* Patients previously enrolled on ACCRN07 are eligible to enroll on Tracking Outcome, Registry and Future Contact components of APEC14B1 any time after they reach age of majority
* Patients with a known or suspected neoplasm that occurs in the pediatric, adolescent or young adult populations are eligible for enrollment as follows:
* All cancer cases with an International Classification of Diseases for Oncology (ICD-O) histologic behavior code of one "1" (borderline), two "2" (carcinoma in situ) or three "3" (malignant)
* All neoplastic lesions of the central nervous system regardless of behavior, i.e., benign, borderline or malignant
* The following other benign/borderline conditions:
* Mesoblastic nephroma
* Teratomas (mature and immature types)
* Myeloproliferative diseases including transient myeloproliferative disease
* Langerhans cell histiocytosis
* Lymphoproliferative diseases
* Desmoid tumors
* Gonadal stromal cell tumors
* Neuroendocrine tumors including pheochromocytoma
* Melanocytic tumors, except clearly benign nevi
* Ganglioneuromas
* Subjects must be =< 25 years of age at time of original diagnosis, except for patients who are being screened specifically for eligibility onto a COG (or COG participating National Clinical Trials Network [NCTN]) therapeutic study, for which there is a higher upper age limit
* All patients or their parents or legally authorized representatives must sign a written informed consent and agree to participate in at least one component of the study; parents will be asked to sign a separate consent for their own biospecimen submission
* If patients or their parents or legally authorized representatives have not signed the Part A subject consent form at the time of a diagnostic bone marrow procedure, it is recommended that they initially provide consent for drawing extra bone marrow using the Consent for Collection of Additional Bone Marrow; consent using the Part A subject consent form must be provided prior to any other procedures for eligibility screening or banking under APEC14B1
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Minimum age
No limit
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Maximum age
25
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
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Study design
Purpose
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Duration
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Selection
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Timing
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Statistical methods / analysis
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Recruitment
Recruitment status
Recruiting
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Data analysis
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Reason for early stopping/withdrawal
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Other reasons
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Date of first participant enrolment
Anticipated
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Actual
3/11/2015
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
Anticipated
31/12/2030
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Actual
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Sample size
Target
33000
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
NSW,QLD,SA,VIC,WA
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Recruitment hospital [1]
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John Hunter Children's Hospital - Hunter Regional Mail Centre
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Sydney Children's Hospital - Randwick
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The Children's Hospital at Westmead - Westmead
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Queensland Children's Hospital - South Brisbane
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Women's and Children's Hospital-Adelaide - North Adelaide
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Monash Medical Center-Clayton Campus - Clayton
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Royal Children's Hospital - Parkville
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Princess Margaret Hospital for Children - Perth
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Perth Children's Hospital - Perth
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2310 - Hunter Regional Mail Centre
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2031 - Randwick
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2145 - Westmead
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Recruitment postcode(s) [4]
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4101 - South Brisbane
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Recruitment postcode(s) [5]
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5006 - North Adelaide
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Recruitment postcode(s) [6]
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3168 - Clayton
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Recruitment postcode(s) [7]
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3052 - Parkville
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Recruitment postcode(s) [8]
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6008 - Perth
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Recruitment postcode(s) [9]
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6009 - Perth
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Recruitment outside Australia
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United States of America
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Alabama
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Alaska
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Arizona
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California
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Colorado
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Connecticut
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Delaware
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San Juan
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Saudi Arabia
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Riyadh
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Funding & Sponsors
Primary sponsor type
Other
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Name
Children's Oncology Group
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Address
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Country
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Other collaborator category [1]
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Government body
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Name [1]
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National Cancer Institute (NCI)
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Address [1]
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Ethics approval
Ethics application status
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Summary
Brief summary
This study gathers health information for 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.
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Trial website
https://clinicaltrials.gov/study/NCT02402244
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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Douglas Hawkins
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Address
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Children's Oncology Group
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Email
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Contact person for scientific queries
No information has been provided regarding IPD availability
What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
No documents have been uploaded by study researchers.
Results not provided in
https://clinicaltrials.gov/study/NCT02402244
Download to PDF