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Informed consent is crucial before a patient participates in a study, ensuring they understand all aspects, including risks and benefits. This process involves a verbal conversation and a detailed written document, which can exceed 20 pages but is designed to be patient-friendly. For patients speaking different languages, consent forms are provided in their native language to guarantee comprehension. When meeting a patient for the first time and suggesting a study, I present this information clearly to facilitate their understanding and informed decision-making.