Late Effects After Treatment in Patients With Previously Diagnosed High-Risk Neuroblastoma
Recruiting in Palo Alto (17 mi)
+98 other locations
TO
Overseen byTara O Henderson
Age: < 65
Sex: Any
Travel: May Be Covered
Time Reimbursement: Varies
Trial Phase: Academic
Waitlist Available
Sponsor: Children's Oncology Group
No Placebo Group
Trial Summary
What is the purpose of this trial?
This research trial studies late effects after treatment in patients with previously diagnosed high-risk neuroblastoma. Studying late effects after treatment may help to decide which treatments for high-risk neuroblastoma are better tolerated with less side effects over time.
Research Team
TO
Tara O Henderson
Principal Investigator
Children's Oncology Group
Eligibility Criteria
Inclusion Criteria
Patients must have been enrolled on COG neuroblastoma biology study ANBL00B1
Patient must have been diagnosed with high-risk neuroblastoma per ANBL00B1 definition
Patient must have been diagnosed on or after January 1, 2000
See 3 more
Treatment Details
Interventions
- Cytology Specimen Collection Procedure (Procedure)
- Laboratory Biomarker Analysis (Procedure)
- Quality-of-Life Assessment (Other)
Participant Groups
1Treatment groups
Experimental Treatment
Group I: Observational (specimen collection)Experimental Treatment3 Interventions
Patients undergo collection of blood and urine samples on day 1. Patients also undergo clinical assessments, laboratory, radiographic, and other ancillary studies on day 1.
Find a Clinic Near You
Research Locations NearbySelect from list below to view details:
UCSF Benioff Children's Hospital OaklandOakland, CA
Blank Children's HospitalDes Moines, IA
Penn State Children's HospitalHershey, PA
Virginia Commonwealth University/Massey Cancer CenterRichmond, VA
More Trial Locations
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Who Is Running the Clinical Trial?
Children's Oncology Group
Lead Sponsor
Trials
467
Patients Recruited
241,000+
National Cancer Institute (NCI)
Collaborator
Trials
14080
Patients Recruited
41,180,000+