Each trial follows a rigorous scientific protocol that defines who can participate, what will be tested, and how results will be measured. All COG-proposed trials are thoroughly vetted before any child is enrolled. This process includes review and approval by COG experts, the National Cancer Institute (NCI), and each participating hospital. This multi-layer process helps ensure patient protection and scientific rigor.
Before a child enrolls, the clinical team will meet with patients and families to explain the trial’s purpose, procedures, risks, and benefits — a process known as informed consent. If you take part in a clinical trial, your safety will be protected through the informed consent process, careful review and approval of the clinical trial protocol, and ongoing monitoring
COG understands that families often hear this information during one of the most difficult times of their lives, and encourages them to ask questions at any point, not just at enrollment. Throughout the trial, each patient’s response to treatment is carefully monitored, with follow-up care continuing after the trial concludes.
Clinical Trial Questions to Ask Your Provider