A Study for the Registry Enrollment of Patients onto the Childhood Cancer Research Network (CCRN) of the Children's Oncology Group

Overview

  • Study type

    Observational
  • Study IDs

  • Describes the nature of a clinical study. Types include:

    • Observational study — observes people and measures outcomes without affecting results.
    • Interventional study (clinical trial) — studies new tests, treatments, drugs, surgical procedures or devices.
    • Medical records research — uses historical information collected from medical records of large groups of people to study how diseases progress and which treatments and surgeries work best.
  • Site IRB
    • Rochester, Minnesota: 08-000030
    NCT ID: NCT01117168
    Sponsor Protocol Number: ACCRN07

About this study

The purpose of this study is to obtain informed consent from parents (or the patient when appropriate) of infants, children, adolescents, and young adults newly diagnosed with cancer to be enrolled onto the registry of the Childhood Cancer Research Network and/or for permission to be contacted in the future to consider participating in research studies.

 

 

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. If you need assistance understanding the eligibility criteria, please contact the study team.

See eligibility criteria

Inclusion Criteria

  • Pre-CCRN Entry
  • All new patients seen in COG member institutions with any of the following diagnoses are eligible
    • All cancer cases with an ICD-O histologic behavior code of  2 (carcinoma in situ) or 3 (malignant)
    • All lesions of the central nervous system regardless of behavior, i.e., benign, borderline or malignant
    • The benign/borderline conditions which will be reportable by agreement shall include
      • Mesoblastic nephroma
      • All teratomas, regardless of locations
      • Theca cell granulosa cell tumor
      • Lymphoproliferative disease
      • Ganglioneuroma
      • Myeloproliferative disease
      • Langerhan's Cell histiocytosis

Participating Mayo Clinic locations

Study statuses change often. Please contact us for help.

Mayo Clinic Location Status Contact

Rochester, Minn.

Mayo Clinic principal investigator

Carola A Arndt, M.D.

Closed-enrolling by invitation

What is this? (?)
"Close"
Not open to everyone who meets the eligibility criteria, but only those invited to participate by the study team.

Contact information:

Cancer Center Clinical Trials Referral Office

855-776-0015

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CLS-20209360

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