Understanding voluntariness of consent in first-in-human cell therapy trials.

Regen Med

Medical Ethics, Department of Clinical Sciences, Faculty of Medicine, Lund University, BMC I12, 22184 Lund, Sweden.

Published: May 2020

Consensus about contents of voluntariness in informed consent is lacking. Core criteria for voluntary consent are needed to ensure voluntariness. This article outlines the multidimensionality of voluntariness and identifies what could reduce voluntariness, especially in first-in-human clinical trials involving cell therapies. In such trials, truly voluntary consent is especially important because: such trials may involve risk of serious harm, while in case of some diseases, eligible patients often have potentially effective therapeutic alternatives; patients considering participation in high-risk first-in-human trials may feel more desperate and some may be dependent on their caregivers, including those in the family; implanted cells cannot be taken out of the patient's body if the patient wants to withdraw.

Download full-text PDF

Source
http://dx.doi.org/10.2217/rme-2019-0126DOI Listing

Publication Analysis

Top Keywords

voluntary consent
8
trials
5
understanding voluntariness
4
consent
4
voluntariness consent
4
consent first-in-human
4
first-in-human cell
4
cell therapy
4
therapy trials
4
trials consensus
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!