Informed consent
Documented understanding of benefits, risks, and alternatives.
Written informed consent should describe expected effects, dissociation, cardiovascular and urologic risks, off-label status, alternatives, and the plan for integration and follow-up. It is renewed if protocol or dosing changes materially.
Related terms
- Off-label use — FDA-approved medications used for non-approved indications.
Definitions are educational and general. They are not medical advice.
Educational use only. The content on this page is provided for general educational purposes and does not constitute medical advice, diagnosis, or treatment. Ketamine and related therapies carry risks and are appropriate only under qualified medical supervision. Always consult a licensed healthcare professional about your individual situation. Information may change as research evolves.