ライフサイエンスコーパス: written informed consent

1 randomly assigned to treatment who provided written informed consent).

2 iagnosed with paracetamol overdose, and gave written informed consent.

3 tional government, and all participants gave written informed consent.

4 asthmatic and four healthy individuals gave written informed consent.

5 y, the ethical committee did not require any written informed consent.

6 ocal ethics committee, and all subjects gave written informed consent.

7 All participants provided written informed consent.

8 Participants (or parents) gave written informed consent.

9 ging of the breast at 7 T, all patients gave written informed consent.

10 with US, performed with ethical approval and written informed consent.

11 e included in this study after they provided written informed consent.

12 utional review board and patients gave their written informed consent.

13 thics committee approval, and all women gave written informed consent.

14 board approval for this study and patients' written informed consent.

15 Participants provided written informed consent.

16 ol (number 1225/2012), and all patients gave written informed consent.

17 ars) (P = .76) were enrolled after obtaining written informed consent.

18 tutional review board, and all subjects gave written informed consent.

19 All patients gave written informed consent.

20 arch ethics committee, and participants gave written informed consent.

21 with institutional review board approval and written informed consent.

22 oved, HIPAA-compliant prospective study with written informed consent.

23 ethics committee, all participants provided written informed consent.

24 ics were approved, and participants provided written informed consent.

25 onal review board, and all participants gave written informed consent.

26 All subjects gave their written informed consent.

27 ision-making and either formal discussion or written informed consent.

28 ard of each center and participants provided written informed consent.

29 tutional review board, and all patients gave written informed consent.

30 red over 5 years in 91 subjects who provided written informed consent.

31 iew committee approved this study and waived written informed consent.

32 tional nature of the procedures and provided written informed consent.

33 onal review board, and all patients provided written informed consent.

34 oval was obtained, and all subjects provided written informed consent.

35 , and 34 patients were examined after giving written informed consent.

36 oved the protocol, and all patients provided written informed consent.

37 lish, and all participating parents provided written informed consent.

38 ommittee approval, and all participants gave written informed consent.

39 oval was obtained, and all patients provided written informed consent.

40 board approved the study; all subjects gave written informed consent.

41 is study was obtained, and each patient gave written informed consent.

42 ethical committee; each participant provided written informed consent.

43 oard approval, and all participants provided written informed consent.

44 All patients provided written informed consent.

45 participating centers, and patients provided written informed consent.

46 All subjects provided written informed consent.

47 risk, not warranting extensive discussion or written informed consent.

48 All patients provided written informed consent.

49 dical ethics committee and all subjects gave written informed consent.

50 Participating women gave written informed consent.

51 regional ethics committee; all patients gave written informed consent.

52 All patients provided written informed consent.

53 roved this retrospective analysis and waived written informed consent.

54 board approved the study; all subjects gave written informed consent.

55 review board, and all participants provided written informed consent.

56 tee approved the study and all patients gave written informed consent.

57 clinical site, and all participants provided written informed consent.

58 ccording to a HIPAA-compliant protocol, with written informed consent.

59 hics approval, and all participants provided written informed consent.

60 All patients gave written informed consent.

61 es approved the study; all participants gave written informed consent.

62 Ethics Committee, and all subjects gave full written informed consent.

63 ics committee, and all participants provided written informed consent.

64 e approved this study, and all subjects gave written informed consent.

65 All volunteers provided written informed consent.

66 HIPAA compliance, and all patients provided written informed consent.

67 prior to study initiation, and patients gave written informed consent.

68 tutional review board, and all subjects gave written informed consent.

69 he study after ethics committee approval and written informed consent.

70 the institutional ethical review board, with written informed consent.

71 ethics committee, and all patients provided written informed consent.

72 Patients gave written informed consent.

73 ts, and/or their legal representatives, gave written informed consent.

74 review board approved; all patients provided written informed consent.

75 his study and waived the need for individual written informed consent.

76 ew board approval, and all participants gave written informed consent.

77 review board approval and all patients gave written informed consent.

78 Patients gave written informed consent.

79 with institutional review board approval and written informed consent.

80 s obtained for this study; all patients gave written informed consent.

81 icenter study, and all participants provided written informed consent.

82 ears; range, 70.4-101.2 years) who had given written informed consent.

83 ttee, and all patients or their parents gave written informed consent.

84 and Declaration Good Clinical Practice with written informed consent.

85 tional government, and all participants gave written informed consent.

86 iew board-approved study after they provided written informed consent.

87 All patients provided written informed consent.

88 All subjects provided written informed consent.

89 and Accountability Act compliant study with written informed consent.

90 ethics committee, and all participants gave written informed consent.

91 ved this retrospective study, with waiver of written informed consent.

92 Participants gave written informed consent.

93 All patients gave written informed consent.

94 ocal ethics committee, and all subjects gave written informed consent.

95 All subjects provided written informed consent.

96 oved the study and all participants provided written informed consent.

97 approved by institutional review boards with written informed consent.

98 All participants provided written informed consent.

99 ethics committee, and all participants gave written informed consent.

100 the patients and the control group provided written informed consent.

101 review board-approved and participants gave written informed consent.

102 review boards, and all participants provided written, informed consent.

103 rd-approved prospective study, with parental written informed consent, 13-MHz 3D three-dimensional US

104 After written informed consent, 221 consecutive patients >/= 5

105 the institutional review board and patients' written informed consent, 531 women with unilateral inva

106 Following written informed consent, a data set of 36 281 mammogram

107 iew board-approved, prospectively conducted (written informed consent acquired), cross-sectional stud

108 olunteers (mean age 31, five were male) gave written informed consent and both of their IONs were ima

109 years; 78% [29] men, 22% [eight] women) gave written informed consent and completed a questionnaire t

110 Materials and Methods Written informed consent and institutional ethics commit

111 Participants gave written informed consent and the study was approved by t

112 secondary progressive MS ) patients provided written informed consent and underwent 3-T MR imaging.

113 diation therapy for prostate cancer provided written informed consent and were enrolled in a prospect

114 4 groups (range, 60.3% to 71.5%) recommended written informed consent, and personal preferences were

115 All subjects provided written informed consent, and the local institutional re

116 Participants gave written informed consent, and the Norwegian committee fo

117 Materials and Methods All subjects provided written informed consent, and the protocol was approved

118 All study participants gave written informed consent, and the study was approved by

119 his retrospective study, all patients signed written informed consent as a requisite to undergo PET/C

120 ts or guardians of all participants provided written informed consent at the time of enrollment.

121 oards approved the study and donors provided written informed consent before death.

122 Participants provide written informed consent before the MR imaging examinati

123 All patients provided written informed consent before the study; the need to o

124 f research that would require disclosure and written informed consent, but data are lacking on the vi

125 consent for participation for any minors and written informed consent for any participants that were

126 review of stem cell donors who had provided written informed consent for stem cell donation and use

127 Patients gave written informed consent for study enrollment, including

128 Patients gave their written informed consent for study enrollment.

129 Written informed consent for study participation was obt

130 All patients provided written informed consent for study participation, the ab

131 Written informed consent for the percutaneous procedure

132 All patients gave written informed consent for the scientific analysis of

133 hods Institutional review board approval and written informed consent from all participants were obta

134 ocal ethics committees on human studies, and written informed consent from all patients was obtained

135 Institutional review board approval and written informed consent from all patients were obtained

136 nstitutional ethics committee approval, with written informed consent from all patients.

137 approved by institutional review board, with written informed consent from all patients.

138 cal ethical committees on human studies, and written informed consent from all subjects was obtained

139 Institutional review board approval and written informed consent from all subjects were obtained

140 institutional review board approval and with written informed consent from all subjects.

141 l ethical committee was obtained, as well as written informed consent from each participant.

142 with research ethics committee approval and written informed consent from each subject, were include

143 from the institutional ethics committee and written informed consent from the patients, 37 patients

144 Materials and Methods Written informed consent in this institutional review bo

145 board-approved HIPAA-compliant protocol with written informed consent, IVIM and DT imaging were perfo

146 tional review board-approved study, with the written informed consent of all patients, two-dimensiona

147 Institutional review board approval and written informed consent of five volunteers and 33 patie

148 Written informed consent of the original study permitted

149 2008, and July 31, 2012, 4512 women provided written informed consent of whom 3977 (88%) were eligibl

150 Patients provided written informed consent, or, at select sites, there was

151 Most of the public favored written informed consent over the most widely advocated

152 We obtained written informed consent postmortem from the next of kin

153 ubjects and their legal representatives gave written informed consent prior to data collection.

154 ation of Helsinki, and all patients provided written informed consent prior to enrollment.

155 Materials and Methods All patients gave written informed consent prior to inclusion in this inst

156 All patients gave written informed consent prior to their examination.

157 he local ethics committee, and patients gave written informed consent prior to their inclusion in the

158 was 5 weeks, and all men were enrolled with written informed consent prior to treatment.

159 All patients provided written informed consent prior to undergoing any study-r

160 review board-approved screening trial, with written informed consent, recruited female patients at e

161 al review board approval and after obtaining written informed consent, SII examinations were performe

162 pective study in which all subjects provided written informed consent, six patients with relapsing-re

163 All subjects provided written informed consent; the study protocol was approve

164 With written informed consent, this institutional review boar

165 Participants provided written informed consent to a protocol that was approved

166 at elevated risk for breast cancer, who gave written informed consent to participate in a study evalu

167 Each subject gave written informed consent to participate in this institut

168 Study participants provided written informed consent to participate in this institut

169 6.6 years +/- 7.7 [standard deviation]) gave written informed consent to participate in this prospect

170 patients had no evidence of having provided written informed consent to participate.

171 as having dementia, and 634 (9.3%) provided written informed consent to participate.

172 Materials and Methods All participants gave written informed consent to undergo brain magnetic reson

173 years) with malignant liver lesions who gave written informed consent underwent preoperative gadoxeti

174 d by the institutional ethics committee, and written informed consent was acquired.

175 Written informed consent was obtained before enrollment.

176 Written informed consent was obtained for all enrolled s

177 Written informed consent was obtained for this ethics co

178 tional review board approved this study, and written informed consent was obtained from 25 symptomati

179 Written informed consent was obtained from 67 consecutiv

180 Written informed consent was obtained from all 80 patien

181 the National Research Ethical Committee, and written informed consent was obtained from all individua

182 h was approved by the local ethics board and written informed consent was obtained from all participa

183 Written informed consent was obtained from all participa

184 roved by the institutional review board, and written informed consent was obtained from all participa

185 iew boards of all participating centers, and written informed consent was obtained from all participa

186 mmittee approved this prospective study, and written informed consent was obtained from all participa

187 Written informed consent was obtained from all participa

188 Written informed consent was obtained from all participa

189 Written informed consent was obtained from all participa

190 approved by the local ethics committee, and written informed consent was obtained from all participa

191 Written informed consent was obtained from all participa

192 +/- SD, 34.3 +/- 6.5 y) were recruited, and written informed consent was obtained from all participa

193 Written informed consent was obtained from all participa

194 and institutional review board approval, and written informed consent was obtained from all participa

195 Written informed consent was obtained from all participa

196 Written informed consent was obtained from all participa

197 roved by the institutional review board, and written informed consent was obtained from all participa

198 Written informed consent was obtained from all participa

199 Written informed consent was obtained from all participa

200 approved by the local ethics committee, and written informed consent was obtained from all patients

201 Written informed consent was obtained from all patients

202 Written informed consent was obtained from all patients

203 Materials and Methods Written informed consent was obtained from all patients

204 Written informed consent was obtained from all patients,

205 Materials and Methods Written informed consent was obtained from all patients,

206 Written informed consent was obtained from all patients,

207 roved by the institutional review board, and written informed consent was obtained from all patients.

208 Written informed consent was obtained from all patients.

209 Written informed consent was obtained from all patients.

210 Written informed consent was obtained from all patients.

211 was approved by the ethics review board, and written informed consent was obtained from all patients.

212 Written informed consent was obtained from all patients.

213 approved by the local ethics committee, and written informed consent was obtained from all patients.

214 ved by the appropriate ethics committee, and written informed consent was obtained from all patients.

215 National Research Ethics Service Committee; written informed consent was obtained from all patients.

216 udy had institutional review board approval; written informed consent was obtained from all patients.

217 dy was approved by our ethics committee, and written informed consent was obtained from all patients.

218 approved by the local ethics committee, and written informed consent was obtained from all patients.

219 Written informed consent was obtained from all patients.

220 roved by the institutional review board, and written informed consent was obtained from all study par

221 had institutional review board approval, and written informed consent was obtained from all study par

222 approved by the local ethics committees, and written informed consent was obtained from all subjects

223 cal ethical committees on human studies, and written informed consent was obtained from all subjects

224 approved by the local ethical committee, and written informed consent was obtained from all subjects

225 Written informed consent was obtained from all subjects,

226 Written informed consent was obtained from all subjects.

227 approved by the local ethical committee, and written informed consent was obtained from all subjects.

228 e multi-institutional HIPAA-compliant study; written informed consent was obtained from all subjects.

229 was obtained for this prospective study, and written informed consent was obtained from all subjects.

230 institutional review board at each site, and written informed consent was obtained from all subjects.

231 by the local institutional review board, and written informed consent was obtained from all subjects.

232 Written informed consent was obtained from all subjects.

233 er and Leiden University Medical Center, and written informed consent was obtained from all subjects.

234 Written informed consent was obtained from all subjects.

235 erformed with ethical review board approval; written informed consent was obtained from all volunteer

236 Written informed consent was obtained from all volunteer

237 rom the John Radcliffe Hospital, Oxford, UK; written informed consent was obtained from each particip

238 approved by the local ethics committee, and written informed consent was obtained from each particip

239 approved by the local ethical committee, and written informed consent was obtained from each particip

240 Written informed consent was obtained from each particip

241 Written informed consent was obtained from each patient.

242 Written informed consent was obtained from each patient.

243 approved by the local ethics committee, and written informed consent was obtained from each patient.

244 Written informed consent was obtained from each subject.

245 Written informed consent was obtained from each subject.

246 Written informed consent was obtained from each subject.

247 approved by the institutional board review; written informed consent was obtained from healthy subje

248 Written informed consent was obtained from patients or t

249 roved by the institutional review board, and written informed consent was obtained from patients.

250 roved by the institutional review board, and written informed consent was obtained from the patient's

251 roved by the institutional review board, and written informed consent was obtained prior to inclusion

252 The vaccine was administered after written informed consent was obtained to complete a scre

253 ctive reading study (the TOMMY trial), after written informed consent was obtained, 8869 women (age r

254 Materials and Methods After written informed consent was obtained, 8869 women (age r

255 Written informed consent was obtained.

256 nal ethics committee approved the study, and written informed consent was obtained.

257 had institutional review board approval, and written informed consent was obtained.

258 Written informed consent was obtained.

259 was approved by the local ethics committee; written informed consent was obtained.

260 was approved by the local ethics committee; written informed consent was obtained.

261 according to the declaration of Helsinki and written informed consent was obtained.

262 Written informed consent was obtained.

263 was institutional review board approved, and written informed consent was obtained.

264 had institutional review board approval, and written informed consent was obtained.

265 eceived institutional review board approval; written informed consent was obtained.

266 imaging datasets were acquired at 3 T after written informed consent was obtained.

267 d by age, and interviews occurred only after written informed consent was obtained.

268 ved by the institutional research board, and written informed consent was obtained.

269 Written informed consent was obtained.

270 roved by the institutional review board, and written informed consent was obtained.

271 Written informed consent was obtained.

272 oved by the institutional review boards, and written informed consent was obtained.

273 approved the prospective study protocol, and written informed consent was obtained.

274 Written informed consent was waived because all the pati

275 Written informed consent was waived by the institutional

276 utional review board approved the study, and written informed consent was waived for patients and was

277 Requirement for written informed consent was waived.

278 approved by the local ethics committee, and written informed consent was waived.

279 Written informed consent was waived.

280 The requirement to obtain written informed consent was waived.

281 institutional review board, and the need for written informed consent was waived.

282 questions in English or siSwati, and provide written informed consent were eligible for the study.

283 e to access a telephone; and able to provide written informed consent were followed up for 2 years.

284 Patients scheduled for PD who gave written informed consent were included and randomized du

285 hods Institutional review board approval and written informed consent were obtained for the Effect of

286 Institutional review board approval and written informed consent were obtained for this HIPAA-co

287 Institutional review board approval and written informed consent were obtained for this HIPAA-co

288 Institutional review board approval and written informed consent were obtained for this HIPAA-co

289 itutional review board approval and parental written informed consent were obtained for this prospect

290 Institutional review board approval and written informed consent were obtained from all patients

291 hods Institutional review board approval and written informed consent were obtained from all subjects

292 roval of the institutional review boards and written informed consent were obtained from each partici

293 search ethics committee approval and patient written informed consent were obtained.

294 Institutional review board approval and written informed consent were obtained.

295 Local ethics committee approval and written informed consent were obtained.

296 Institutional review board approval and written informed consent were obtained.

297 Institutional review board and written informed consent were obtained.

298 hods Institutional review board approval and written informed consent were obtained.

299 oard and local ethics committee approval and written informed consent were obtained.

300 proved by the institutional review board and written informed consent with HIPAA authorization was ob