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Registration and Informed Consent Study for the Childhood Cancer Research Network

NCT00433394 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 2242

Last updated 2013-06-27

No results posted yet for this study

Summary

RATIONALE: Collecting informed consent from parents of children with cancer to register with the Childhood Cancer Research Network may help the study of cancer in the future.

PURPOSE: This study is collecting informed consent to register younger patients with cancer into the Childhood Cancer Research Network.

Conditions

  • Unspecified Childhood Solid Tumor, Protocol Specific

Interventions

PROCEDURE

cancer prevention intervention

PROCEDURE

educational intervention

Sponsors & Collaborators

  • National Cancer Institute (NCI)

    collaborator NIH

  • Children's Oncology Group

    lead NETWORK

Principal Investigators

  • Julie A. Ross, PhD · Masonic Cancer Center, University of Minnesota

Study Design

Allocation
NA
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Max Age
20 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2001-05-31
Primary Completion
2007-01-31
Completion
2011-01-31

Countries

  • United States
  • Canada

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00433394 on ClinicalTrials.gov