Robert J Levine
Dados Biográficos
| ID | 5138233 |
|---|---|
| NOME | Robert J Levine |
| PRENOMES | Robert J |
| SOBRENOME | Levine |
| ASSINATURA | LEVINE R J |
| AFILIAÇÕES | Yale University |
| VERIFICADO | Não |
| TOTAL DE OBRAS | 44 |
| TOTAL DE CITAÇÕES | 4 |
| TOTAL COMO AUTOR | 44 |
| TOTAL COMO EDITOR | 0 |
| PRIMEIRO ANO DE PUBLICAÇÃO | 1970 |
| ANO MAIS RECENTE DE PUBLICAÇÃO | 2013 |
| ÍNDICE H | 1 |
Criminalization of HIV Transmission and Exposure
More than half of US jurisdictions have laws criminalizing knowing exposure to or transmission of HIV, yet little evidence supports these laws’ effectiveness in reducing HIV incidence. These laws may undermine prevention efforts outlined in the US National HIV/AIDS Strategy, in which the United States has invested substantial federal funds. Future research should include studies of (1) the impact of US HIV exposure laws on public health systems a…
Empirical Research to Evaluate Ethics Committees' Burdensome and Perhaps Unproductive Policies and Practices
THE U.S. SYSTEM FOR THE PROTECTION of human research subjects, particularly its ethics committee or Institutional Review Board (IRB) component, is excessively burdened. Many commentators, myself included, are concerned that, as a consequence of these excessive burdens, the IRB is losing its effectiveness in safeguarding the rights and welfare of human subjects. I believe that IRBs devote too much time doing work that simply does not need to be do…
Research ethics for mental health science involving ethnic minority children and youths
In response to U.S. Public Health Service projects promoting attention to disparities in the outcomes of mental health treatments, in July 2001, the American Psychological Association, the National Institute of Mental Health, and the Fordham University Center for Ethics Education convened a group of national leaders in bioethics, multicultural research, and ethnic minority mental health to produce a living document to guide ethical decision makin…
Demystifying Central Review Boards
Robert J. Levine, Louis Lasagna, Demystifying Central Review Boards: Current Options and Future Directions: A Summary Report of Outcomes from "Central IRB Review of Multi-Site Trials," 27-28 October 1998, IRB: Ethics & Human Research, Vol. 22, No. 6 (Nov. - Dec., 2000), pp. 1-9
Proposed Regulations for Research Involving Those Institutionalized as Mentally Infirm
Robert J. Levine, Proposed Regulations for Research Involving Those Institutionalized as Mentally Infirm: A Consideration of Their Relevance in 1996, IRB: Ethics & Human Research, Vol. 18, No. 5 (Sep. - Oct., 1996), pp. 1-5
[Treating the Troops]
Building a New Consensus
Carol Levine, Nancy Neveloff Dubler, Robert J. Levine, Building a New Consensus: Ethical Principles and Policies for Clinical Research on HIV / AIDS, IRB: Ethics & Human Research, Vol. 13, No. 1/2 (Jan. - Apr., 1991), pp. 1-17
Such a Bargain
The Doctor's Unproven Beliefs and the Subject's Informed Choice
An IRB-Approved Protocol on the Use of Human Fetal Tissue
Research with Human Subjects
Ackerman reviews three recent books on moral issues in human research: Who Goes First? The Story of Self-Experimentation in Medicine, by Lawrence K. Altman (Random House; 1987); The Patient as Partner: A Theory of Human-Experimentation Ethics, by Robert M. Veatch (Indiana University Press; 1987); and Ethics and Regulation of Clinical Research, 2d ed., by Robert J. Levine (Urban & Schwarzenberg; 1986)
Community consultation in socially sensitive research
Community consultation in socially sensitive research
[The Doctor's Unproven Beliefs and the Subject's Informed Choice]
Should I Enroll in a Randomized Clinical Trial? Excerpts from a Patient's Guide
FDA's New Rule on Treatment Use and Sale of Investigational New Drugs
[How Many Subjects Are Required for a Study?]
Case Studies
Anthony Breuer, Robert J. Levine, George A. Kanoti, Douglas P. Lackey, Case Studies: Can a Healthy Subject Volunteer to Be Injured in Research?, The Hastings Center Report, Vol. 16, No. 4 (Aug., 1986), pp. 31-33
Research That Could Yield Marketable Products from Human Materials
Commentary
The Use of Placebos in Randomized Clinical Trials
Most discussions of the ethical problems presented by the use of placebos in randomized clinical trials focus on the problem of deception. As I shall demonstrate, this focus is misplaced; it reflects a lack of appreciation of the differences between placebo usage in medical practice and in randomized clinical trials. One class of placebo usage in randomized clinical trials presents peculiarly difficult ethical problems-that is, clinical trials in…
What Kinds of Subjects Can Understand This Protocol
Inconsistency and IRBs
Research Involving Children
Research on Prisoners
The debate over whether prisoners should be allowed to volunteer to be research subjects has consumed the time and energy of many responsible and thoughtful people during the past three decades. I have published a survey of the major themes in these arguments.' Now I wish we could lay this issue to rest. In my view there is no good reason to prevent prisoners who wish to volunteer for most types of research from doing so. After World War II, the …
Criminalization of HIV Transmission and Exposure
More than half of US jurisdictions have laws criminalizing knowing exposure to or transmission of HIV, yet little evidence supports these laws’ effectiveness in reducing HIV incidence. These laws may undermine prevention efforts outlined in the US National HIV/AIDS Strategy, in which the United States has invested substantial federal funds. Future research should include studies of (1) the impact of US HIV exposure laws on public health systems a…
Empirical Research to Evaluate Ethics Committees' Burdensome and Perhaps Unproductive Policies and Practices
THE U.S. SYSTEM FOR THE PROTECTION of human research subjects, particularly its ethics committee or Institutional Review Board (IRB) component, is excessively burdened. Many commentators, myself included, are concerned that, as a consequence of these excessive burdens, the IRB is losing its effectiveness in safeguarding the rights and welfare of human subjects. I believe that IRBs devote too much time doing work that simply does not need to be do…
Studies on the Role of Acid in the Pathogenesis of Experimental Stress Ulcers
Previous studies have provided strong evidence to support the concepts that in the rat histamine is the chemical mediator of gastric acid secretion and that histamine plays an essential role in the pathogenesis of stress ulcers. The present experiments indicate that the role of histamine in the pathogenesis of stress ulcers in rats is probably mediated through stimulation of gastric acid secretion. In particular, we found a strong negative correl…
Clarifying the Concepts of Research Ethics
O ne of the most important achievements of the National Commission for the Protection of Human Subjects of Biomedical and Behavioral Research (the Commission) was to begin the process of correcting the conceptual and semantic errors that had undermined virtually all previous attempts to develop rational public policy on research involving human subjects. The fruits of this achievement are seen most clearly in the later reports of the Commission-o…
Therapeutic and Nontherapeutic Research
Advice on Compensation
What Should Consent Forms Say about Cash Payments
Changing Federal Regulation of IRBs, Part II
Deceiving Dentists
Advice on Compensation
Changing Federal Regulation of IRBs
Commentary
Commentary
Medical Students as Social Scientists
The Senate's Proposed Statutory Definition of 'Voluntary and Informed Consent
Can (Or Should) the IRB Assume the FDA's Functions at Early Stages of the IND Process
What Should Subjects Be Told about Withdrawing from a Protocol
Commentary
Research on Prisoners
The debate over whether prisoners should be allowed to volunteer to be research subjects has consumed the time and energy of many responsible and thoughtful people during the past three decades. I have published a survey of the major themes in these arguments.' Now I wish we could lay this issue to rest. In my view there is no good reason to prevent prisoners who wish to volunteer for most types of research from doing so. After World War II, the …
According to Protocol
Consent to Incomplete Disclosure as an Alternative to Deception
What Are the IRB's Obligations to Review the Use of Drugs for Purposes That FDA Has Not Approved
Research Involving Children
What Kinds of Subjects Can Understand This Protocol
Inconsistency and IRBs
Commentary
The Use of Placebos in Randomized Clinical Trials
Most discussions of the ethical problems presented by the use of placebos in randomized clinical trials focus on the problem of deception. As I shall demonstrate, this focus is misplaced; it reflects a lack of appreciation of the differences between placebo usage in medical practice and in randomized clinical trials. One class of placebo usage in randomized clinical trials presents peculiarly difficult ethical problems-that is, clinical trials in…
Medicine (25 obras) · Psychology (25 obras) · Political science (14 obras) · Computer Science (11 obras) · Business (9 obras) · Law (9 obras) · Biomedical Ethics and Regulation (8 obras) · Alternative medicine (7 obras) · Engineering (7 obras) · Ethics in Clinical Research (7 obras)