| informed consent |
when appropriate information is provided in order to enable patients to make decisions which reflect their own values. Health professionals subscribe to the values of non-directive counselling and informed consent, in order that patients can make decisions which are best for them, on the basis of full and balanced information. ...
출처: www.antenataltesting.info/glossary.html
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| informed consent |
A discussion of the procedures, risks, and benefits of a clinical trial between the investigator and the patient. All patients must sign the informed consent form before participating in a trial.
출처: www.ccfa.org/trials/glossary
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| informed consent |
The process in which a patient learns about and understands the purpose and aspects of a clinical trial and then agrees to participate. Of course, a patient may decline to participate. This process includes a document defining how much a patient must know about the potential benefits and risks of therapy before being able to agree to undergo it knowledgeably. (Informed consent is required in federally conducted, funded or regulated studies a swell as by many state laws. ...
출처: www.womens-wellness.com/Glossary.html
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| informed consent |
The voluntary verification of a patient's willingness to participate in a clinical trial, along with the documentation thereof. This verification is requested only after complete, objective information has been given about the trial, including an explanation of the study's objectives, potential benefits, risks and inconveniences, alternative therapies available, and of the subject's rights and responsibilities in accordance with the current revision of the Declaration of Helsinki.
출처: www.wcctrials.com/glossary.HTM
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| informed consent |
A process by which a subject voluntarily confirms his or her willingness to participate in a particular trial, after having been informed of all aspects of the trial that are relevant to the subject
출처: www.brentwoodresearch.com/glossary.cfm
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