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List of works by David Wendler

"Targeted" consent for pragmatic clinical trials

scientific article

A Framework for Risk-Benefit Evaluations in Biomedical Research ⬇️

scientific article published on June 1, 2011

A New Justification for Pediatric Research Without the Potential for Clinical Benefit ⬇️

scientific article published on January 1, 2012

A Proposed Process for Reliably Updating the Common Rule

scientific article

A Response to Commentators on "Should Children Decide Whether They Are Enrolled in Nonbeneficial Research?"

journal article; published in The American Journal of Bioethics in 2003

A family's request for complementary medicine after patient brain death

scientific article published on May 2008

A new method for making treatment decisions for incapacitated patients: what do patients think about the use of a patient preference predictor?

scientific article published on 29 January 2016

A pragmatic analysis of vulnerability in clinical research

scientific article published on September 2017

A proposal and prototype for a Research Risk Repository to improve the protection of research participants ⬇️

scientific article published on August 22, 2011

A standard for assessing the risks of pediatric research: pro and con.

scientific article

Acceptable Approaches to Enrolling Adults Who Cannot Consent in More Than Minimal Risk Research

scientific article published on October 2015

Addressing exploitation of poor clinical trial participants in North America and the European Union

scientific article published on 14 July 2016

Adolescent Research Participants' Descriptions of Medical Research

scientific article published on 19 February 2015

Ancillary care obligations of medical researchers

scientific article published in July 2009

Are physicians obligated always to act in the patient's best interests?

scientific article published in February 2010

Are racial and ethnic minorities less willing to participate in health research?

scientific article

Assent in research: the voices of adolescents

scientific article

Assessing the ethical and practical wisdom of surrogate consent for living organ donation

scientific article published in The Journal of the American Medical Association

Assessing the ethics of ethics research: a case study.

scientific article

Authors' Reply

Benefits and burdens of participation in a longitudinal clinical trial

scientific article

Broad Consent for Research With Biological Samples: Workshop Conclusions

scientific article

Broad Consent for Research on Biospecimens: The Views of Actual Donors at Four U.S. Medical Centers

scientific article published in January 2018

Broad versus blanket consent for research with human biological samples

scientific article

Can We Improve Treatment Decision-Making for Incapacitated Patients?

scientific article published on 01 September 2010

Can we ensure that all research subjects give valid consent?

scientific article published in November 2004

Challenging the Sanctity of Donorism: Patient Tissue Providers as Payment-Worthy Contributors

scientific article published in January 2015

Children's and their parents' views on facing research risks for the benefit of others

scientific article published on 01 January 2008

Clarifying and defending the endorsed life approach to surrogate decision-making

scientific article published on 28 July 2015

Clarifying substituted judgement: the endorsed life approach

scientific article published on 30 October 2014

Clinical research: Should patients pay to play?

scientific article published on July 2015

Clinician Integrity and Limits to Patient Autonomy ⬇️

scientific article published on February 2, 2011

Commentary: Should the Belmont Report Be Extended to Animal Research

scientific article published on 01 January 2020

Comparative effectiveness research: what to do when experts disagree about risks

scientific article

Conducting human challenge studies in LMICs: A survey of researchers and ethics committee members in Thailand

scientific article published on 10 October 2019

Confronting Ethical and Regulatory Challenges of Emergency Care Research With Conscious Patients

scientific article published on 18 December 2015

Consent for Pragmatic Trials in Acute Myocardial Infarction

scientific article published on 01 March 2018

Consent for research with biological samples: one-time general consent versus a gift model

scientific article published on April 2012

Considerations in the evaluation and determination of minimal risk in pragmatic clinical trials

scientific article

Contrasting views of risk perception and influence of financial compensation between adolescent research participants and their parents

scientific article published on 17 December 2014

Debriefing and accountability in deceptive research.

scientific article published in September 2008

Deception in research on the placebo effect

scientific article

Deception in the pursuit of science

scientific article published in March 2004

Declaration of Helsinki and protection for vulnerable research participants--reply

scientific article published in March 2014

Direct-to-consumer advertising and physician prescribing

scientific article published on 01 August 2005

Disclosure of Incidental Findings From Next-Generation Sequencing in Pediatric Genomic Research ⬇️

scientific article published on February 11, 2013

Dissolving the dilemma over forced treatment

scientific article published in April 2005

Do Patients Want their Families or their Doctors to Make Treatment Decisions in the Event of Incapacity, and Why?

scientific article published on 26 April 2016

Do U.S. regulations allow more than minor increase over minimal risk pediatric research? Should they?

scientific article

Does it matter whether investigators intend to benefit research subjects?

scientific article

Does random treatment assignment cause harm to research participants?

scientific article (publication date: June 2006)

Empirical evaluation of the need for 'on-going consent' in clinical research

scientific article

Ensuring Respect for Human Research Participants: Institutional Review Boards and Sharing Results From Research

scientific article published on September 2016

Ethical issues in denial of church wedding based on couple's hemoglobin genotype in Enugu, south eastern Nigeria

scientific article published on 29 May 2019

Evaluating the risks of clinical research

scientific article published on October 2010

Evaluating the risks of clinical research: direct comparative analysis

scientific article

Examining the ethics of clinical use of unproven interventions outside of clinical trials during the Ebola epidemic

scientific article published in January 2015

Hematopoietic stem cell transplant research with pediatric donors: when can institutional review boards approve it?

scientific article published on June 2006

How do children and parents make decisions about pediatric clinical research?

scientific article published in November 2008

How do institutional review boards apply the federal risk and benefit standards for pediatric research?

scientific article published on January 2004

How does the collection of genetic test results affect research participants?

scientific article published in August 2007

How should treatment decisions be made for incapacitated patients, and why?

scientific article published in March 2007

How to Enroll Participants in Research Ethically ⬇️

scientific article published on April 20, 2011

In Defense of a Social Value Requirement for Clinical Research

scientific article published on February 2017

Informed consent for research and authorization under the Health Insurance Portability and Accountability Act Privacy Rule: an integrated approach

scientific article

Informed consent: practices and views of investigators in a multinational clinical trial

article

Innovative approaches to informed consent for randomized clinical trials: Identifying the ethical challenges

scientific article published in December 2017

Institutional review board practices regarding assent in pediatric research

scientific article published on June 2004

International Guidelines and Ethical Context

Interpretation of the subjects' condition requirement: a legal perspective

scientific article published on January 2010

Involving Communities in Deciding What Benefits They Receive in Multinational Research

scientific article

Is emergency research without initial consent justified?: the consent substitute model

scientific article published on April 2010

Is it important to disclose how treatments are selected in clinical research and clinical care?

scientific article published on 3 April 2017

Is it possible to protect pediatric research subjects without blocking appropriate research?

scientific article published on April 2008

Is the French clinical trials regulation discriminatory?

scientific article published on 09 August 2016

Is there a role for assent or dissent in animal research?

scientific article published on 01 October 2015

Justice and nontherapeutic pediatric research

scientific article published in January 2014

Locating the Source(s) of the Social Value Requirement(s)

scientific article published on 01 November 2018

Making the transition to a learning health care system. Commentary

scientific article

Making treatment decisions for oneself: weighing the value

scientific article

Medical decision making for patients without surrogates

scientific article published on September 2007

Minimal risk in pediatric research

scientific article published on 01 December 2006

Minimal risk in pediatric research as a function of age.

scientific article published on February 2009

Must research participants understand randomization?

scientific article published in February 2009

Nonbeneficial research with individuals who cannot consent: is it ethically better to enroll healthy or affected individuals?

scientific article published in July 2003

One-time general consent for research on biological samples

scientific article

One-time general consent for research on biological samples: is it compatible with the health insurance portability and accountability act?

scientific article published on July 2006

Overcoming language barriers in medical care

scientific article published on 01 November 2006

Palliative care: a supportive adjunct to pediatric phase I clinical trials for anticancer agents?

scientific article published on 01 September 2004

Patients' beliefs regarding informed consent for low-risk pragmatic trials

scientific article published on 18 September 2017

Patients' priorities for treatment decision making during periods of incapacity: quantitative survey

scientific article published on 2 October 2014

Placebo research and the spirit of informed consent

scientific article published in July 2005

Post-trial Access to Tested Interventions: The Views of IRB/REC Chair, Investigators, and Research Participants in a Multinational HIV/AIDS Study

article

Pragmatic Randomized Trials Without Standard Informed Consent?: A National Survey.

scientific article published on 28 July 2015

Protecting communities in health research from exploitation

article

Protecting subjects who cannot give consent: toward a better standard for "minimal" risks

scientific article published on 01 September 2005

Protections for clinical trials in low and middle income countries need strengthening not weakening

scientific article

Public preferences on written informed consent for low-risk pragmatic clinical trials in Spain

scientific article published on 16 April 2017

Quality of parental consent in a Ugandan malaria study

scholarly article by Christine Pace et al published July 2005 in American Journal of Public Health

Quantifying the federal minimal risk standard: implications for pediatric research without a prospect of direct benefit.

scientific article

Quantifying the risks of non-oncology phase I research in healthy volunteers: meta-analysis of phase I studies

scientific article

Reconsidering the Need for Reconsent at 18

scientific article published on 06 July 2018

Reframing Consent for Clinical Research: A Function-Based Approach

scientific article published in December 2017

Research advance directives: protection or obstacle?

scientific article published on December 2005

Research benefits for hypothetical HIV vaccine trials: The views of Ugandans in the Rakai District.

scientific article published on March 2008

Research involving pediatric stem cell donors: A way forward

scientific article published on 17 February 2016

Research involving wards of the state: protecting particularly vulnerable children

scientific article

Research on stored biological samples: the views of Ugandans.

scientific article published on March 2005

Research on stored biological samples: views of African American and White American cancer patients

scientific article

Research with stored biological samples: what do research participants want?

scientific article

Response to open peer commentaries on "Must research participants understand randomization?"

Risk standards for pediatric research: rethinking the Grimes ruling.

scientific article published in June 2004

Risks of phase I research with healthy participants: A systematic review

scientific article published on 8 September 2015

Shared medical decision‐making: considering what options to present based on an ethical analysis of the treatment of brain tumors in very young children ⬇️

scientific article published on April 22, 2012

Should all research subjects be treated the same?

scientific article published on January 2015

Should children decide whether they are enrolled in nonbeneficial research?

scientific article published in January 2003

Should protections for research with humans who cannot consent apply to research with nonhuman primates?

scientific article

Systematic Review: Individuals' Goals for Surrogate Decision‐Making ⬇️

scientific article published on 03 April 2012

Systematic Review: The Effect on Surrogates of Making Treatment Decisions for Others ⬇️

scientific article published on March 1, 2011

Taking the measure of the therapeutic misconception ⬇️

scientific article published on December 1, 2012

Targeted Consent for Research on Standard of Care Interventions in the Emergency Setting

scientific article published on 9 August 2016

The 50th anniversary of the Declaration of Helsinki: progress but many remaining challenges

scientific article

The Guinea Phase III Ebola Vaccine Trial: Lessons for Research Ethics Review in Public Health Emergencies

article

The Moral Duty to Buy Health Insurance ⬇️

scientific article published on July 11, 2012

The Permissibility of Deception in Riskier Research

scientific article published on 01 March 2020

The Potential Benefits of Research May Justify Certain Research Risks

scientific article published on 20 February 2019

The Potential for Infrastructure Benefits and the Responsiveness Requirement

scientific article published on June 2016

The Quality of Informed Consent in a Clinical Research Study in Thailand

scientific article published on 01 January 2005

The Theory and Practice of Surrogate Decision-Making

scientific article published on 01 January 2017

The Value in Doing Something

scientific article published on 01 February 2019

The accuracy of surrogate decision makers: a systematic review

scientific article published in March 2006

The ethics of paying for children's participation in research

scientific article published in August 2002

The ethics of peer review in bioethics

scientific article published on 16 October 2013

The ethics of phase 0 oncology trials

scientific article published in June 2008

The ethics of sham invasive intervention trials

scientific article published on 01 October 2009

The ethics of studying subjects in non-ideal circumstances ⬇️

scientific article published on July 1, 2012

The potential exploitation of research participants in high income countries who lack access to health care

scientific article published on 6 January 2016

The relevance of empirical research in bioethics

scientific article published on 28 September 2005

The standard of care debate: can research in developing countries be both ethical and responsive to those countries' health needs?

article

Three steps to protecting pediatric research participants from excessive risks

scientific article published on 29 September 2006

Treatment decision making for incapacitated patients: is development and use of a patient preference predictor feasible?

scientific article published on 20 February 2014

Understanding preferences regarding consent for pragmatic trials in acute care

scientific article published on 03 October 2018

Use of a patient preference predictor to help make medical decisions for incapacitated patients

scientific article published on 13 February 2014

Using Data to Improve Surrogate Consent for Clinical Research with Incapacitated Adults ⬇️

scientific article published on April 1, 2012

Using mobile location data in biomedical research while preserving privacy

article

Views of Adolescents and Parents on Pediatric Research Without the Potential for Clinical Benefit ⬇️

scientific article published on September 10, 2012

What is a "minor" increase over minimal risk?

scientific article published on 01 November 2005

What makes clinical research in developing countries ethical? The benchmarks of ethical research

scientific article

What research with stored samples teaches us about research with human subjects

scientific article published in February 2002

What should be disclosed to research participants?

scientific article

What should research participants understand to understand they are participants in research?

scientific article

What we worry about when we worry about the ethics of clinical research

scholarly article published June 2011

When Research Regulations and Ethics Conflict

journal article; published in The American Journal of Bioethics in 2018

When clinical care is like research: the need for review and consent

scientific article published on 17 May 2016

When do the federal regulations allow placebo-controlled trials in children?

scientific article

Which alternatives should investigators disclose to research subjects?

scientific article

Which benefits of research participation count as 'direct'?

scientific article

Why is Coerced Consent Worse Than No Consent and Deceived Consent?

scientific article published in April 2017

Why patients continue to participate in clinical research

scientific article

Why we need legal standards for pediatric research

scientific article published on 01 February 2004

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