Use of altered informed consent in pragmatic clinical research.
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Stakeholders' views on the ethical challenges of pragmatic trials investigating pharmaceutical drugs.Pragmatic Trials in Maintenance Dialysis: Perspectives from the Kidney Health Initiative.The Comprehensive Post-Acute Stroke Services (COMPASS) study: design and methods for a cluster-randomized pragmatic trial.Harmonization and streamlining of research oversight for pragmatic clinical trialsThe Food and Drug Administration and pragmatic clinical trials of marketed medical products.The ethics and regulatory landscape of including vulnerable populations in pragmatic clinical trials.Considerations in the evaluation and determination of minimal risk in pragmatic clinical trials.Exploring the ethical and regulatory issues in pragmatic clinical trials.Examining Provisions Related to Consent in the Revised Common Rule.PRagmatic trial Of Video Education in Nursing homes: The design and rationale for a pragmatic cluster randomized trial in the nursing home setting.Recruiting to preclinical Alzheimer's disease clinical trials through registries.Physicians' perspectives regarding pragmatic clinical trials.Proposals to Conduct Randomized Controlled Trials Without Informed Consent: a Narrative Review.Pragmatic clinical trials embedded in healthcare systems: generalizable lessons from the NIH Collaboratory.Patients' beliefs regarding informed consent for low-risk pragmatic trials.Willingness to participate in pragmatic dialysis trials: the importance of physician decisional autonomy and consent approach.Reframing Consent for Clinical Research: A Function-Based Approach.Ethical issues in pragmatic randomized controlled trials: a review of the recent literature identifies gaps in ethical argumentation.Sources of Safety Data and Statistical Strategies for Design and Analysis: Real World Insights.Capacity, Vulnerability, and Informed Consent for Research.Ensuring respect for persons in COMPASS: a cluster randomised pragmatic clinical trialWhere Did Informed Consent for Research Come From?Developing a framework for the ethical design and conduct of pragmatic trials in healthcare: a mixed methods research protocol
P2860
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P2860
Use of altered informed consent in pragmatic clinical research.
description
2015 nî lūn-bûn
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2015年の論文
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2015年学术文章
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2015年学术文章
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2015年学术文章
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2015年学术文章
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2015年学术文章
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2015年學術文章
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2015年學術文章
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2015年學術文章
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name
Use of altered informed consent in pragmatic clinical research.
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Use of altered informed consent in pragmatic clinical research.
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type
label
Use of altered informed consent in pragmatic clinical research.
@ast
Use of altered informed consent in pragmatic clinical research.
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prefLabel
Use of altered informed consent in pragmatic clinical research.
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Use of altered informed consent in pragmatic clinical research.
@en
P2093
P2860
P356
P1433
P1476
Use of altered informed consent in pragmatic clinical research.
@en
P2093
Bray Patrick-Lake
Brian Rath
Daniel E Ford
Hollie Schmidt
John D Lantos
Jonathan McCall
Kevin Weinfurt
Mark J Pletcher
Ross E McKinney
P2860
P304
P356
10.1177/1740774515597688
P577
2015-09-15T00:00:00Z