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Observational (specimen collection) for Neuroblastoma
N/A
Waitlist Available
Led By Tara O Henderson
Research Sponsored by Children's Oncology Group
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be younger than 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to 3 years
Awards & highlights
Summary
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.
Eligible Conditions
- Neuroblastoma
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ up to 3 years
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to 3 years
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Pediatric Quality of Life (PedsQL) score
Prevalence of specific late effects
Risk factors of late effects
Secondary outcome measures
Collection and storage of blood samples
Trial Design
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.
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Who is running the clinical trial?
Children's Oncology GroupLead Sponsor
457 Previous Clinical Trials
239,454 Total Patients Enrolled
63 Trials studying Neuroblastoma
31,500 Patients Enrolled for Neuroblastoma
National Cancer Institute (NCI)NIH
13,841 Previous Clinical Trials
41,002,439 Total Patients Enrolled
205 Trials studying Neuroblastoma
53,319 Patients Enrolled for Neuroblastoma
Tara O HendersonPrincipal InvestigatorChildren's Oncology Group
1 Previous Clinical Trials
1,875 Total Patients Enrolled
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