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1
What should be disclosed to research participants?
Am J Bioeth. 2013;13(12):3-8. doi: 10.1080/15265161.2013.851578.
2
Randomization should be disclosed to potential research subjects.
Am J Bioeth. 2013;13(12):35-7. doi: 10.1080/15265161.2013.849307.
3
The "research misconception" and the SUPPORT trial: toward evidence-based consensus.
Am J Bioeth. 2013;13(12):48-50. doi: 10.1080/15265161.2013.851297.
4
Risk, respect for persons, and informed consent in comparative effectiveness research.
Am J Bioeth. 2013;13(12):46-8. doi: 10.1080/15265161.2013.851299.
5
What are reasonably foreseeable risks?
Am J Bioeth. 2013;13(12):29-30. doi: 10.1080/15265161.2013.849304.
6
The weird divergence of ethics and regulation with regard to informed consent.
Am J Bioeth. 2013;13(12):31-3. doi: 10.1080/15265161.2013.849308.
7
Ensuring transparency: presenting the trade-offs between the research treatment options.
Am J Bioeth. 2013;13(12):50-2. doi: 10.1080/15265161.2013.852272.
8
Understanding randomization: helpful strategies.
Am J Bioeth. 2009 Feb;9(2):14-5. doi: 10.1080/15265160802663245.
9
Randomization can be risky.
Am J Bioeth. 2009 Feb;9(2):17-8. doi: 10.1080/15265160802668954.
10
Equipoise trumps randomization.
Am J Bioeth. 2009 Feb;9(2):13-4. doi: 10.1080/15265160902802610.

引用本文的文献

1
Exploring the ethics of tuberculosis human challenge models.
J Med Ethics. 2023 Dec 30. doi: 10.1136/jme-2023-109234.
4
Details of risk-benefit communication in informed consent documents for phase I/II trials.
Clin Trials. 2021 Feb;18(1):71-80. doi: 10.1177/1740774520971770. Epub 2020 Nov 24.
5
Informed consent disclosure to vaccine trial subjects of risk of COVID-19 vaccines worsening clinical disease.
Int J Clin Pract. 2021 Mar;75(3):e13795. doi: 10.1111/ijcp.13795. Epub 2020 Dec 4.
6
Informational needs for participation in bioequivalence studies: the perspectives of experienced volunteers.
Eur J Clin Pharmacol. 2019 Nov;75(11):1575-1582. doi: 10.1007/s00228-019-02738-6. Epub 2019 Aug 19.
9
Patients' Views Concerning Research on Medical Practices: Implications for Consent.
AJOB Empir Bioeth. 2016;7(2):76-91. doi: 10.1080/23294515.2015.1117536. Epub 2015 Nov 16.
10
A comparison of institutional review board professionals' and patients' views on consent for research on medical practices.
Clin Trials. 2016 Oct;13(5):555-65. doi: 10.1177/1740774516648907. Epub 2016 Jun 1.

本文引用的文献

1
The OHRP and SUPPORT--another view.
N Engl J Med. 2013 Jul 11;369(2):e3. doi: 10.1056/NEJMc1308015. Epub 2013 Jun 26.
2
The OHRP and SUPPORT.
N Engl J Med. 2013 Jun 20;368(25):e36. doi: 10.1056/NEJMc1307008. Epub 2013 Jun 5.
3
In support of SUPPORT--a view from the NIH.
N Engl J Med. 2013 Jun 20;368(25):2349-51. doi: 10.1056/NEJMp1306986. Epub 2013 Jun 5.
5
Can research and care be ethically integrated?
Hastings Cent Rep. 2011 Jul-Aug;41(4):37-46. doi: 10.1002/j.1552-146x.2011.tb00123.x.
6
Target ranges of oxygen saturation in extremely preterm infants.
N Engl J Med. 2010 May 27;362(21):1959-69. doi: 10.1056/NEJMoa0911781. Epub 2010 May 16.
7
Are physicians obligated always to act in the patient's best interests?
J Med Ethics. 2010 Feb;36(2):66-70. doi: 10.1136/jme.2009.033001.
8
Does random treatment assignment cause harm to research participants?
PLoS Med. 2006 Jun;3(6):e188. doi: 10.1371/journal.pmed.0030188.
9
Systematic review to determine whether participation in a trial influences outcome.
BMJ. 2005 May 21;330(7501):1175. doi: 10.1136/bmj.330.7501.1175.

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