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CLINICAL TRIAL: STUDY DESIGN Randomized Controlled Trial of a Mobile Clinical Decision Aid to Improve Access to Kidney Transplantation: choose Kidney Rachel E. Patzer1, Joshua Basu1, Suit Mohan2,

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What is clinical trial study design?

Clinical trial study design is the plan or blueprint outlining how a clinical trial will be conducted, including the methodology, objectives, endpoints, treatment allocation, and statistical analysis.

Who is required to file clinical trial study design?

Researchers conducting clinical trials are required to submit the study design to regulatory authorities for approval before beginning the trial.

How to fill out clinical trial study design?

Researchers can fill out the clinical trial study design by providing detailed information on the trial protocol, study objectives, methods, endpoints, inclusion/exclusion criteria, statistical analysis plan, and ethical considerations.

What is the purpose of clinical trial study design?

The purpose of the clinical trial study design is to ensure that the trial is conducted in a scientifically valid and ethical manner, with clear objectives, methods, and endpoints.

What information must be reported on clinical trial study design?

The clinical trial study design should include information on the trial protocol, study objectives, methodology, statistical analysis plan, treatment allocation, endpoints, and ethical considerations.

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