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2 it exceeds the risk, and 3) patients are fully informed and consent, can adhere to follow-up, and alert providers to hepa
3 tionships with communities may increase acceptance of broad consent and wide data sharing in biobank research.
5 cenarios: tiered consent and controlled data sharing; broad consent and controlled data sharing; or broad consent and ope
6 The most common reason given for endorsing the deferred consent process was the stress of the early ICU experience 25
8 This scoping review of the literature on requesting family consent was prepared to support of the development of leading
11 titutional review board approval was obtained, and informed consent was waived in this HIPAA-compliant retrospective stud
14 ndemnity payments, malpractice lawsuits, including informed consent allegations, still present a time, money, and reputat
15 er, there is a paucity of literature investigating informed consent in spinal surgery malpractice.
19 centre, found to have inadequate documentation of informed consent, immediately withdrew consent, or randomly assigned t
20 Kidney transplant candidates (KTCs) must provide informed consent to accept kidneys from increased risk donors (IRD), b
21 football players (age range, 52-65 years) provided informed consent to participate in this cross-sectional study.
23 was approved by the local ethics board and written informed consent was obtained from all participants.
26 ved by the institutional review board, and written informed consent was obtained from all study participants.
27 pproved by the institutional board review; written informed consent was obtained from healthy subjects and was waived for
29 ds Institutional review board approval and written informed consent were obtained for the Effect of Iso-osmolar Contrast
30 ds Institutional review board approval and written informed consent were obtained from all subjects.
31 aterials and Methods All subjects provided written informed consent, and the protocol was approved by the university inst
40 anagement of uncertainty, the extent of donor and recipient consent, the scope of the obligation that the organization ha
42 qualify for a waiver of the consent requirements, targeted consent's verbal disclosure is preferable to waiving consent,
43 For trials that qualify for a waiver of the consent requirements, targeted consent's verbal disclosure is
44 ly allocated to one of three hypothetical scenarios: tiered consent and controlled data sharing; broad consent and contro
45 rgeted consent's verbal disclosure is preferable to waiving consent, provided a slight delay is consistent with appropria
46 There has been significant debate over what consent process, if any, should be used for clinical trials t
48 One patient (in the FST group) withdrew consent before drug administration and was excluded from anal
49 ate documentation of informed consent, immediately withdrew consent, or randomly assigned to intervention groups in error
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