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Informed Consent

Meaning

Informed consent is the ethical and legal prerequisite in clinical practice where a patient, possessing full comprehension of a proposed diagnostic procedure or therapeutic intervention, voluntarily authorizes its undertaking. For hormonal health protocols, this demands a clear explanation of the risks, benefits, alternatives, and expected physiological outcomes associated with treatments like TRT or specialized supplementation. The clinician bears the responsibility to ensure the patient understands complex endocrinological concepts sufficiently to make an autonomous decision. This process validates patient autonomy within the therapeutic relationship.