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Book
Identification and Estimation of Local Average Treatment Effects
Authors: --- ---
Year: 1995 Publisher: Cambridge, Mass. National Bureau of Economic Research

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Abstract

We investigate conditions sufficient for identification of average treatment effects using instrumental variables. First we show that the existence of valid instruments is not sufficient to identify any meaningful average treatment effect. We then establish that the combination of an instrument and a condition on the relation between the instrument and the participation status is sufficient for identification of a local average treatment effect for those who can be induced to change their participation status by changing the value of the instrument. Finally we derive the probability limit of the standard IV estimator under these conditions. It is seen to be a weighted average of local average treatment effects.


Book
Rethinking the ethics of clinical research : widening the lens.
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ISBN: 9780199743513 Year: 2011 Publisher: Oxford Oxford university press

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Search the studies - NIH clinical research studies.
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Publisher: Bethesda, MD : NIH Clinical Center, National Institutes of Health

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Book
Guidance for industry : M3 nonclinical safety studies for the conduct of human clinical trials for pharmaceuticals.
Authors: ---
Year: 1997 Publisher: Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research : Center for Biologics Evaluation and Research,

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Book
Sources of Identifying Information in Evaluation Models
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Year: 1991 Publisher: Cambridge, Mass. National Bureau of Economic Research

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The average effect of social programs on outcomes such as earnings is a parameter of primary interest in econometric evaluations studies. New results on using exclusion restrictions to identify and estimate average treatment effects are presented. Identification is achieved given a minimum of parametric assumptions, initially without reference to a latent index framework. Most econometric analyses of evaluation models motivate identifying assumptions using models of individual behavior. Our technical conditions do not fit easily into a conventional discrete choice framework, rather they fit into a framework where the source of identifying information is institutional knowledge regarding program administration. This framework also suggests an attractive experimental design for research using human subjects, in which eligible participants need not be denied treatment. We present a simple instrumental variables estimator for the average effect of treatment on program participants, and show that the estimator attains Chamberlain's semi-parametric efficiency bound. The bias of estimators that satisfy only exclusion restrictions is also considered.


Book
Recruiting human subjects : sample guidelines for practice.
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Year: 2000 Publisher: [Washington, D.C.] : Department of Health and Human Services, Office of Inspector General,

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Book
Recruiting human subjects : pressures in industry-sponsored clinical research.
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Year: 2000 Publisher: [Washington, D.C.] : Department of Health and Human Services, Office of Inspector General,

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Periodical
Updating the Common Rule in an era of big health data
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Year: 2019 Publisher: [Washington, D.C.] : Congressional Research Service,

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Book
Guidance for industry : M3 nonclinical safety studies for the conduct of human clinical trials for pharmaceuticals.
Authors: ---
Year: 1997 Publisher: Rockville, MD : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Drug Evaluation and Research : Center for Biologics Evaluation and Research,

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Book
Recruiting human subjects : sample guidelines for practice.
Author:
Year: 2000 Publisher: [Washington, D.C.] : Department of Health and Human Services, Office of Inspector General,

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