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Northeastern UniversityLearn More: Protecting Human Subjects Participating in Research and their Personal Privacy + NIH Clinical Trial & Common Rule UpdatesRESEARCH ADMINISTRATION November 2017Northeastern
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How to fill out cancer clinical trial participants

01
Research and identify a cancer clinical trial that you are eligible for.
02
Contact the trial coordinator or research team to express interest in participating.
03
Schedule a screening appointment to determine if you meet the eligibility criteria.
04
Review and sign the informed consent form.
05
Follow the trial protocol and attend all required appointments and follow-up visits.

Who needs cancer clinical trial participants?

01
Hospitals and research institutions conducting cancer clinical trials need participants to test the safety and efficacy of new treatments.
02
Patients with cancer who are seeking alternative or advanced treatment options may also benefit from participating in clinical trials.
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Cancer clinical trial participants are individuals who are enrolled in research studies to test new treatments or interventions for cancer.
Researchers conducting the clinical trials are required to file information on the participants.
Researchers must provide detailed information about the participants, including their demographics, medical history, treatment received, and outcomes.
The purpose of cancer clinical trial participants is to evaluate the safety and effectiveness of new cancer treatments.
Information such as age, gender, cancer type, treatment received, side effects, and outcomes must be reported on cancer clinical trial participants.
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