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Comprehensive Cancer Center of Wake Forest University CROP RESEARCH BASECCCWFU #60A02 A Phase II Randomized Placebo Controlled, Double Blinded Trial to Evaluate the Effects of Fruit and Vegetable
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Administer the assigned treatments to participants as per the protocol, ensuring compliance with the study procedures.
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Collect data on various endpoints, such as efficacy measures, safety parameters, and any other relevant outcomes specified in the study protocol.
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A phase II randomized study is a clinical trial where participants are randomly assigned to different treatment groups to compare the effectiveness and safety of different interventions.
Researchers conducting clinical trials are required to file a phase II randomized study.
To fill out a phase II randomized study, researchers must follow the protocol set out in the study design and accurately record data on participant outcomes and adverse events.
The purpose of a phase II randomized study is to evaluate the efficacy and safety of a new intervention or treatment in a controlled setting before moving on to larger-scale clinical trials.
Information that must be reported on a phase II randomized study includes participant demographics, treatment assignment, outcomes, adverse events, and follow-up data.
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