000 01159 a2200313 4500
005 20250517103332.0
264 0 _c20171130
008 201711s 0 0 eng d
022 _a1740-7753
024 7 _a10.1177/1740774516656945
_2doi
040 _aNLM
_beng
_cNLM
100 1 _aChen, Stephanie C
245 0 0 _aA framework for analysis of research risks and benefits to participants in standard of care pragmatic clinical trials.
_h[electronic resource]
260 _bClinical trials (London, England)
_c12 2016
300 _a605-611 p.
_bdigital
500 _aPublication Type: Journal Article; Research Support, N.I.H., Intramural
650 0 4 _aBiomedical Research
_xethics
650 0 4 _aEthics, Research
650 0 4 _aHumans
650 0 4 _aInformed Consent
650 0 4 _aPragmatic Clinical Trials as Topic
650 0 4 _aResearch Subjects
650 0 4 _aRisk Assessment
650 0 4 _aStandard of Care
650 0 4 _aUnited States
700 1 _aKim, Scott Yh
773 0 _tClinical trials (London, England)
_gvol. 13
_gno. 6
_gp. 605-611
856 4 0 _uhttps://doi.org/10.1177/1740774516656945
_zAvailable from publisher's website
999 _c26178080
_d26178080