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Memorial Sloan Kettering Cancer Center IRB Number: 18199 A(3) Approval date: 18Sep2018PARTICIPANT INFORMED CONSENT FOR CLINICAL RESEARCH Study Title for Study Participants: Overnight Fasting After
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How to fill out cancer clinical trials
How to fill out cancer clinical trials
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Research and find a clinical trial that is suitable for your type and stage of cancer.
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Participate in the informed consent process, where you will receive detailed information about the trial and its risks and benefits.
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Follow the trial protocol and attend all required appointments and procedures as outlined in the study.
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Keep a detailed record of any symptoms or side effects experienced during the trial and report them to the research team.
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Complete the trial as per the study protocol and follow-up with the research team for any long-term follow-up care.
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Individuals diagnosed with cancer who are interested in exploring alternative treatment options or experimental therapies.
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What is cancer clinical trials?
Cancer clinical trials are research studies that involve people to test new treatments or procedures to find better ways to prevent, diagnose, or treat cancer.
Who is required to file cancer clinical trials?
Researchers and organizations conducting the clinical trials are required to file cancer clinical trials.
How to fill out cancer clinical trials?
To fill out cancer clinical trials, researchers need to provide detailed information about the study design, participants, interventions, outcomes, and ethical considerations.
What is the purpose of cancer clinical trials?
The purpose of cancer clinical trials is to improve cancer treatment and care by testing new therapies and interventions.
What information must be reported on cancer clinical trials?
Information such as study protocol, participant data, adverse events, and outcomes must be reported on cancer clinical trials.
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