| informed consent |
consent by a patient to undergo a medical or surgical treatment or to participate in an experiment after the patient understands the risks involved
출처: wordnet.princeton.edu/perl/webwn
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| informed consent |
A process in which a person learns key facts about a clinical trial, including potential risks and benefits, before deciding whether or not to participate in a study. Informed consent continues throughout the trial.
출처: www.stjude.org/glossary
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| informed consent |
The permission granted by a participant in a research study (including medical research) after he/she has received comprehensive information about the study. This is a statement of trust between the institution performing the research procedure and the person (eg, a patient) on whom the research procedures are to be performed. This includes the type of protection available to people considering entering a drug trial. ...
출처: www.amfar.org/cgi-bin/iowa/bridge.html
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| informed consent |
The process by which a healthcare provider gives a patient information, including pros and cons, about a potential new treatment; when a person is entering a clinical trial, that person must sign a document with this information, thereby providing "informed consent."
출처: www.thebody.com/hivnews/aidscare/dec97/pullout.htm...
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| informed consent |
Disclosure of a certain amount of information to the patient about the proposed treatment and the attainment of the patient's consent, which must be competent, understanding, and voluntary.
출처: www.dphilpotlaw.com/html/glossary.html
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