ライフサイエンスコーパス: research protocol

1 splants are currently permitted only under a research protocol.

2 ries from 0 through 10 days depending on the research protocol.

3 als (HIV+), provided it is performed under a research protocol.

4 appreciation of the information concerning a research protocol.

5 aluate individuals' capacity to consent to a research protocol.

6 res can be used under a compassionate-use or research protocol.

7 tion-approved biopsy system and not within a research protocol.

8 ent according to an institutionally approved research protocol.

9 for CDKN2A should be done only as part of a research protocol.

10 rolled in a prospective, strict weight loss, research protocol.

11 ts answered a questionnaire relating to each research protocol.

12 mon to include SPECT imaging in clinical and research protocols.

13 from initial submission to final approval of research protocols.

14 ms, rather then having them being limited to research protocols.

15 or inclusion of critically ill patients into research protocols.

16 capacity to consent to clinical treatment or research protocols.

17 judges of the burdens and risks of specific research protocols.

18 first-line platinum-based chemotherapy or in research protocols.

19 mandatory single-time review for multicenter research protocols, additional financial support for IRB

20 ndees at community meetings for an emergency research protocol and determine whether these meetings a

21 objective measurement tools with transparent research protocols and data reduction strategies would a

22 These global data might help guide research protocols and prioritisation efforts and focus

23 , risk from nontherapeutic components of the research protocol, and the psychological impact of parti

24 on-making to determine study direction, plan research protocols, and conduct project activities.

25 Special scrutiny recognizes that not all research protocols are equally ethically challenging and

26 Standardized phytosanitary measures and research protocols are needed to improve the flow of inf

27 757 volunteers who were participating in our research protocols at the Mayo Clinic between 1995 and 2

28 , relapsed, and refractory SAA in 3 separate research protocols at the National Institutes of Health.

29 esonance images from men who participated in research protocols at the Veterans Affairs Palo Alto Hea

30 Differences in interlaboratory research protocols contribute to the conflicting data in

31 ided whenever possible within the context of research protocols designed to evaluate clinical outcome

32 recent literature and our large personal and research protocol experience of bone marrow failure in t

33 informed, 66% reported participating in the research protocol for personal reasons, and 34% reported

34 The detailed know-how to implement research protocols frequently remains restricted to the

35 ymptom assessed during administration of the research protocol, had used alcohol and/or other drugs w

36 information on organization, governance, and research protocols; half address institutional review bo

37 ls, it might be successfully done outside of research protocols if attention is paid to selection, ed

38 ingly utilized in clinical management and in research protocols in the approach to DME.

39 In a research protocol involving autozygome mapping and exome

40 comorbidity in both clinical assessment and research protocols involving children with ADHD.

41 diction tool envisioned to be most useful in research protocols involving the psychosis prodrome.

42 noma should, whenever possible, occur within research protocols, it might be successfully done outsid

43 Although research protocols may take as long as 60-90 min, much m

44 Our research protocol measured blood pressure noninvasively

45 All participants underwent a research protocol MRI, and 41% were classified as having

46 To advance the state of the science, research protocols need to provide more explicit rationa

47 lingness to participate in four hypothetical research protocols of varying risk/benefit profiles were

48 e are as a group able to distinguish between research protocols of varying risk/benefit profiles.

49 under the minimal risk threshold; and 5) the research protocol provides sufficient latitude for treat

50 ence exists that patients who participate in research protocols (PRP) significantly differ from nonpa

51 rd investigators who fully disseminate their research protocols, reports, and participant-level datas

52 herapy, cardiogenic shock, and enrollment in research protocols requiring 4 weeks of ticlopidine were

53 ontext of standard clinical practice and the research protocol, risks must be minimized, potential be

54 ther than the ovary, and future clinical and research protocols should employ thorough examination of

55 th the participant consent agreement and the research protocol submitted to the IRB.

56 tumors and were subsequently entered into a research protocol that consisted of accelerated radiatio

57 ly studied as part of a pre-existing ongoing research protocol to evaluate the effects of maternal ma

58 for cancer susceptibility in two structured research protocols to accurately anticipate emotional re

59 The animal research protocol was approved by the Institutional Anim

60 This research protocol was approved by the institutional revi

61 Research protocol was HIPAA compliant and approved by in

62 Four hypothetical research protocols were rated.

63 V-positive transplantations will occur under research protocols with safeguards and criteria mandated

64 can be incorporated into survey and pedigree research protocols without hindering projects with exten