Ignite Creation Date:
2024-05-05 @ 5:21 PM
Last Modification Date:
2024-10-26 @ 9:30 AM
Study NCT ID:
NCT00433394
Status:
COMPLETED
Last Update Posted:
2013-06-27
First Post:
2007-02-09
Brief Title:
Registration and Informed Consent Study for the Childhood Cancer Research Network
Sponsor:
Childrens Oncology Group
Organization:
Childrens Oncology Group
Study Overview
Official Title:
Protocol for Registration and Consent to the Childhood Cancer Research Network - A Limited Institution Pilot
Status:
COMPLETED
Status Verified Date:
2013-06
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief 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
PURPOSE This study is collecting informed consent to register younger patients with cancer into the Childhood Cancer Research Network
Detailed Description:
OBJECTIVES
Obtain informed consent from parents and the child when appropriate of children diagnosed with cancer who are under 21 years of age to register their childs name and address with the Childhood Cancer Research Network
Obtain informed consent from parents and the child when appropriate of children diagnosed with cancer who are under 21 years of age to be contacted in the future for possible participation in non-therapeutic research studies involving the parents andor child
Facilitate the systematic registration of pediatric and adolescent patients diagnosed with cancer into the Childhood Cancer Research Network
OUTLINE Consent is obtained from parents and pediatric patients where applicable to register the patients and parents names and addresses with the Childhood Cancer Research Network provide a copy of the pathology report to the Network and contact parents in the future for possible non-therapeutic research studies involving the parents andor child
Information provided will be held in strict confidence
PROJECTED ACCRUAL Not specified
Obtain informed consent from parents and the child when appropriate of children diagnosed with cancer who are under 21 years of age to register their childs name and address with the Childhood Cancer Research Network
Obtain informed consent from parents and the child when appropriate of children diagnosed with cancer who are under 21 years of age to be contacted in the future for possible participation in non-therapeutic research studies involving the parents andor child
Facilitate the systematic registration of pediatric and adolescent patients diagnosed with cancer into the Childhood Cancer Research Network
OUTLINE Consent is obtained from parents and pediatric patients where applicable to register the patients and parents names and addresses with the Childhood Cancer Research Network provide a copy of the pathology report to the Network and contact parents in the future for possible non-therapeutic research studies involving the parents andor child
Information provided will be held in strict confidence
PROJECTED ACCRUAL Not specified
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None
Secondary IDs
| Secondary ID | Type | Domain | Link |
|---|---|---|---|
| COG-AADM01P1 | OTHER | Childrens Oncology Group | None |