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1 in the area for 3 or more years, and able to provide informed consent.
2 nts or their proxies may not be available to provide informed consent.
3 OP at 1 of 6 major ROP centers whose parents provided informed consent.
4 -controlled clinical trial, and all patients provided informed consent.
5 All subjects provided informed consent.
6 nd their candidacy for surgical intervention provided informed consent.
7 All participants provided informed consent.
8 onal review board approval, and all subjects provided informed consent.
9 All study patients provided informed consent.
10 ard approval, and patients in the CLQ cohort provided informed consent.
11 ved the study protocol, and all participants provided informed consent.
12 s; age range, 47-81 years) were enrolled and provided informed consent.
13 tutional review board approval; participants provided informed consent.
14 itutional review board approval and patients provided informed consent.
15 All subjects provided informed consent.
16 Patients provided informed consent.
17 nderwent screening FFDM during 2004-2013 and provided informed consent.
18 ethics committee, and all 20 adult patients provided informed consent.
19 d at each screening center; all participants provided informed consent.
20 titutional review board and each participant provided informed consent.
21 All study participants provided informed consent.
22 pproved the study protocol, and all patients provided informed consent.
23 institutional review board, and all subjects provided informed consent.
24 the local ethics committee, and all patients provided informed consent.
25 s prospective single-arm study, and patients provided informed consent.
26 tutional review board approval; all patients provided informed consent.
27 oved the HIPAA-compliant study; all patients provided informed consent.
28 institutional review board; all participants provided informed consent.
29 All participants provided informed consent.
30 Patients provided informed consent.
31 All patients provided informed consent.
32 board approved this study, and all subjects provided informed consent.
33 All subjects provided informed consent.
34 MR-guided focused ultrasound ablation after providing informed consent.
35 went echo-planar spectroscopic imaging after providing informed consent.
36 derwent standard ophthalmic evaluation after providing informed consent.
37 help in developing more effective methods of providing informed consent.
41 S (eight men, two women; mean age, 41 years) provided informed consent and underwent 3.0-T MR imaging
42 25 years, in good general health, willing to provide informed consent, and were not pregnant or breas
43 HIV, were not too impaired to comprehend and provide informed consent, and, for this paper, who teste
46 aging Network National CT Colonography Trial provided informed consent, and approval was obtained fro
49 atory response; pain caused by cIAI; able to provide informed consent; and diagnosis of cIAI with son
51 ability of individuals with schizophrenia to provide informed consent for research has become the foc
52 with schizophrenia and subjects with HIV to provide informed consent for research participation and
54 subjects with at least one CAD risk factor) provided informed consent for participation in this inst
57 oard-approved study, all patients with ADPKD provided informed consent; for control subjects, informe
59 urteen age- and sex-matched control subjects provided informed consent in accordance with the institu
60 erials and Methods Thirty recruited patients provided informed consent in this institutional review b
62 mmography Registry between 2006 and 2012 and provided informed consent or a waiver for research, in c
63 the exclusion criteria were being unable to provide informed consent, or being too ill or distressed
64 research is whether participants are able to provide informed consent, particularly for protocols ent
65 estions about suicidal patients' capacity to provide informed consent, the risk of some lethal outcom
67 ioning, psychiatric symptoms, and ability to provide informed consent to a hypothetical drug trial.
68 Kidney transplant candidates (KTCs) must provide informed consent to accept kidneys from increase
69 atric symptoms and cognitive dysfunction can provide informed consent to participate in research is a
70 D) grade U (unclassified) or grade I-IV COPD provided informed consent to an ethics board-approved HI
71 ods Eighteen patients with biopsy-proven PCa provided informed consent to be included in this institu
72 prior mammograms and additional risk factors provided informed consent to enroll in an institutional
73 al football players (age range, 52-65 years) provided informed consent to participate in this cross-s
79 y volunteers (median age, 22.5 years), after providing informed consent, underwent MR imaging while m
80 ho spoke either English or Luganda and could provide informed consent were eligible for participation
82 ts at Eastern State Hospital in Kentucky who provided informed consent were genotyped at the CYP2D6 l
83 omputed tomographic (CT) angiography and who provided informed consent were prospectively randomized
86 to hospital in the past 36h; and (d) able to provide informed consent will be eligible to participate
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