informed consent


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Related to informed consent: Informed Consent Form

informed consent

n.
Consent by a person to undergo a medical procedure, participate in a clinical trial, or be counseled by a professional such as a social worker or lawyer, after receiving all material information regarding risks, benefits, and alternatives.

informed′ consent′


n.
a patient's consent to a medical or surgical procedure or to participation in a clinical study after being properly advised of the relevant medical facts and the risks involved.
[1965]
ThesaurusAntonymsRelated WordsSynonymsLegend:
Noun1.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
consent - permission to do something; "he indicated his consent"
Translations

in·form·ed con·sent

n. consentimiento informado.
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References in periodicals archive ?
NZNO IS again running its popular medico-legal forums in 2018, this time on the topic of informed consent.
Toms, a recent landmark decision on informed consent, is correct?
Informed consent "denotes the agreement by a person to a proposed course of conduct after the lawyer has communicated adequate information and explanation about the material risks of and reasonably available alternatives to the proposed course of conduct.
Informed Consent: Written informed consent was obtained from the patient for publication of this case report and accompanying images.
With these thoughts in mind, I take a fresh and provocative look at the accepted paradigm of informed consent in clinical and research settings.
Patient's informed consent is a legal document and a moral principle.
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Question: Which of the following statements regarding the doctrine of informed consent is best?
A few years ago our doctor, who is an alternative doctor, and others worked with the state legislature to get an informed consent form for patients to sign.
Informed consent letters clarify that the CPA advises and informs, and the client decides.
Informed consent is a basic ethical requirement in biomedical research involving human subjects.