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  • clinical trial
  • A health care provider may ask a patient to consent to receive therapy before providing it, or a clinical researcher may ask a research participant before enrolling that person into a clinical trial . (wikipedia.org)
  • Additional requirements for federally funded studies - For each clinical trial conducted or supported by a Federal department or agency, one IRB approved informed consent form must be posted to a publicly available Federal website (yet to be specified) after the trial is closed to recruitment and no later than 60 days after the last study visit by any subject. (mclaren.org)
  • basic
  • Impairments to reasoning and judgment that may prevent informed consent include basic intellectual or emotional immaturity, high levels of stress such as posttraumatic stress disorder (PTSD) or a severe intellectual disability , severe mental disorder , intoxication , severe sleep deprivation , Alzheimer's disease , or being in a coma . (wikipedia.org)
  • In taking on these broad basic challenges, it hopes to inform medical education and cost-effective medical practice in modern medical settings as well. (tghn.org)
  • person
  • The person requesting the action may honestly be unaware of this and believe the consent is genuine, and rely on it. (wikipedia.org)
  • human
  • Consent may be implied within the usual subtleties of human communication, rather than explicitly negotiated verbally or in writing. (wikipedia.org)