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期刊名:Ajob empirical bioethics

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ISSN:2329-4515

e-ISSN:2329-4523

IF/分区:0.0/

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共收录本刊相关文章索引269
Clinical Trial Case Reports Meta-Analysis RCT Review Systematic Review
Classical Article Case Reports Clinical Study Clinical Trial Clinical Trial Protocol Comment Comparative Study Editorial Guideline Letter Meta-Analysis Multicenter Study Observational Study Randomized Controlled Trial Review Systematic Review
Georgia Lowe,Jonathan Pugh,Guy Kahane et al. Georgia Lowe et al.
Background: Increasing use of genetic technologies in clinical and research settings increases the potential for misattributed paternity to be identified. Yet existing guidance from the President's Commission for the Stud...
Anya E R Prince,R Jean Cadigan,Warren Whipple et al. Anya E R Prince et al.
This pilot study reports on a survey regarding recruitment, appointment, and training of members for health care ethics committees (HCECs). Background: Pa...
Rahul K Nayak,David Wendler Rahul K Nayak
Background: Current practice and policies maintain that it is very important to disclose to potential research subjects that their treatment will be selected by randomization. In contrast, it typically is not considered i...
Amber Rose Comer,Margaret Gaffney,Cynthia L Stone et al. Amber Rose Comer et al.
Background: Although state surrogate laws are the most common way surrogate decision makers are identified, no studies have been conducted to determine physician understanding of these laws or how these laws are utilized ...
Robert D Annett,Janet L Brody,David G Scherer et al. Robert D Annett et al.
Purpose: Voluntary consent/assent with adolescents invited to participate in research raises challenging problems. No studies to date have attempted to manipulate autonomy in relation to assent/consent processes. This stu...
George E Hardart,Matthew K Labriola,Kenneth Prager et al. George E Hardart et al.
Background: Despite calls for a controlled organ donation after circulatory death (cDCD) consent process that is more rigorous, consistent, and transparent, little is known about the cDCD consent processes utilized by U.S...
Emily E Anderson,Susan B Newman,Alicia K Matthews Emily E Anderson
Purpose: Innovation will be required to improve the informed consent process in research. We aimed to obtain input from key stakeholders-research participants and those responsible for obtaining informed consent-to inform...
Brian C Martinson,David C Mohr,Martin P Charns et al. Brian C Martinson et al.
Background: Assessing the integrity of research climates and sharing such information with research leaders may support research best practices. We report here results of a pilot trial testing the effectiveness of a repor...
Katrina Hauschildt,Trisha K Paul,Raymond De Vries et al. Katrina Hauschildt et al.
Background: Although a mechanism for resolving ethical issues in patient care is required for accreditation of American hospitals, there are no formal qualifications for providing clinical ethics consultation (CEC), and t...
Amelia S Knopf,Amy Lewis Gilbert,Gregory D Zimet et al. Amelia S Knopf et al.
Background: Biomedical HIV prevention research with minors is complicated by the requirement of parental consent, which may disclose sensitive information to parents. We examine the experience of principal investigators (...