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Effect of informed consent on patient characteristics in a stroke thrombosis trial Thomas, MD Florent Boutique, PhD John B. Tieback, MD Claus Z. Simon sen, MD, PhD Norbert Nighoghossian, MD Salvador
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Informed consent is an ethical and legal concept which requires that individuals are provided with all relevant information and options before making a decision or giving their consent to a particular treatment or procedure.
Healthcare providers are required to ensure that informed consent is obtained from their patients before any medical treatment or procedure.
Informed consent forms are typically filled out by the healthcare provider and the patient, with the healthcare provider ensuring that all necessary information is provided.
The purpose of informed consent is to protect the autonomy of the patient and ensure that they have the necessary information to make an informed decision about their medical care.
The informed consent form must include information about the nature of the treatment or procedure, the potential risks and benefits, and any alternative options available.
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