1000 Participants Needed

Data Registry for Pediatric Cancer

Recruiting at 19 trial locations
GB
SM
AM
BE
Overseen ByBCC Enroll
Age: Any Age
Sex: Any
Trial Phase: Academic
Sponsor: Giselle SaulnierSholler
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

This trial aims to gather information and specimens from children and young people with cancer, helping researchers understand more about these diseases. It does not involve any new treatments; instead, it collects data and samples to support future research on childhood cancers. This trial could suit those diagnosed with childhood cancer, survivors, or even healthy individuals willing to contribute. Participants must consent to the use of their data and samples for research purposes.

As an unphased trial, this study offers a unique opportunity for participants to contribute to groundbreaking research that could shape future cancer treatments.

Do I have to stop taking my current medications for this trial?

The trial information does not specify whether you need to stop taking your current medications. It is best to discuss this with the trial coordinators or your doctor.

Why are researchers excited about this trial?

Researchers are excited about the Beat Childhood Cancer Specimen Banking and Data Registry because it aims to gather crucial data that could transform how pediatric solid tumors are understood and treated. Unlike current treatments that primarily focus on attacking the tumors directly, this registry collects and analyzes biological samples and clinical information to uncover patterns and insights into the disease. This approach has the potential to accelerate the development of more personalized and effective therapies, ultimately improving outcomes for children with these challenging conditions.

Who Is on the Research Team?

GS

Giselle Sholler, MD

Principal Investigator

Beat Childhood Cancer at Atrium Health

Are You a Good Fit for This Trial?

Inclusion Criteria

I have given my written consent to participate.
My age does not limit my participation.
I am healthy or have conditions not related to the study's focus.
See 3 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Data Collection and Specimen Banking

Collection of clinical and genomic data, and banking of specimens for research

10 years

Follow-up

Participants are monitored for safety and effectiveness after data collection

10 years

What Are the Treatments Tested in This Trial?

Interventions

  • No intervention- registry only

How Is the Trial Designed?

1

Treatment groups

Experimental Treatment

Group I: Patients with suspected or confirmed pediatric solid tumorsExperimental Treatment1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Giselle SaulnierSholler

Lead Sponsor

Trials
22
Recruited
2,400+

Giselle Sholler

Lead Sponsor

Trials
23
Recruited
2,500+

Wake Forest University Health Sciences

Lead Sponsor

Trials
1,432
Recruited
2,506,000+