Individually-Randomized Controlled Trials of Vaccines Against the Next Outbreak

Guest Post: Nir Eyal, Marc Lipsitch Paper: Vaccine testing for emerging infections: the case for individual randomisation  The humbling experience of international response to Ebola taught the world a thing or two on preparing for Zika and for other emerging infections. Some of those lessons pertain to vaccine development against emerging infections. One lesson was […]

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The Deadly Business of an Unregulated Global Stem Cell Market

Guest Post: The deadly business of an unregulated global stem cell industry Tereza Hendl and Tamra Lysaght In our paper, we report on the case of a 75-year old Australian woman who died in December 2013 from complications of an autologous stem cell procedure. This case was tragic and worth reporting to the medical ethics community […]

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How to Keep HIV Cure-Related Trials Ethical: The Benefit/Risk Ratio Challenge

Guest Post by Nir Eyal Re: Special Issue of the Journal of Medical Ethics on the ethics and challenges of an HIV cure For most patients with HIV who have access to antiretroviral treatment and use it properly, that treatment works well. But the holy grail of HIV research remains finding a cure. Sometimes that […]

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HIV Cure Research and The Dual Aims of the Informed Consent Process

Guest Post: Danielle Bromwich and Joseph Millum Paper: Informed Consent to HIV Research  Special Issue: The benefit/risk ratio challenge in clinical research, and the case of HIV cure A cure for HIV would be tremendously valuable. Approximately 37 million people worldwide are HIV-positive and 15 million are currently on antiretroviral therapy. Until recently it was assumed […]

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A Hot Take on a Cold Body

It’s good to see Nils’ post about the recent UK cryonics ruling getting shared around quite a bit – so it should.  I thought I’d throw in my own voice, too. About 18 months ago, Imogen Jones and I wrote a paper musing on some of the ethical and legal dimensions of Christopher Priest’s The Prestige. […]

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Dissenting from care.data: an analysis of opt out forms

Guest Post: Paraskevas Vezyridis Article: Dissenting from Care.data: An Analysis of Opt-out Forms In our article, which is part of a wider project examining the technical, social and ethical challenges of big data in primary care, we simply wanted to explore how varied opt out forms can be when there is no standardised form available. […]

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The End is Not What it Seems – Feasibility of Conducting Prospective Research in Critically Ill, Dying Patients.

Guest Post by Amanda Van Beinum Re: Feasibility of conducting prospective observational research on critically ill, dying patients in the intensive care unit Collecting information about how people die in the intensive care unit is important. Observations about what happens during the processes of withdrawal of life sustaining therapies (removal of breathing machines and drugs used to maintain […]

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Where to Publish and Not to Publish in Bioethics

Guest Post by Stefan Eriksson & Gert Helgesson, Uppsala University * Note: this is a cross-posting from The Ethics Blog, hosted by the Centre for Research Ethics & Bioethics (CRB) at Uppsala University. The link to the original article is here. Re-posted with permission of the authors. Introduction Allegedly, there are over 8,000 so-called predatory […]

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Circumcision and Sexual Function: Bad Science Reporting Misleads Parents

by Brian D. Earp / (@briandavidearp) Introduction Another day, another round of uncritical media coverage of an empirical study about circumcision and sexual function. That’s including from the New York Times, whose Nicholas Bakalar has more or less recycled the content of a university press release without incorporating any skeptical analysis from other scientists. That’s par for […]

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A Tool to Help Address Key Ethical Issues in Research

Guest post by Rebecca H. Li and Holly Fernandez Lynch One of the most important responsibilities of a clinical project lead at a biotech company or an academic research team is to generate clinical trial protocols. The protocol dictates how a trial will be conducted and details background information on prior research, scientific objectives, study […]

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