Part I of this Comment traces the development of ethical and legal guidelines for current informed consent procedures. Part II outlines the extent of parental authority in volunteering children for research, including legal exceptions to parental permission and possible limitations imposed on parental rights by the courts. Part III challenges the assumption that parents can and will always act in their child\u27s best interest. Part IV argues that institutional review boards cannot be relied upon to protect children when parents fail to do so. Finally, Part V proposes possible improvements to the problematic evaluation process of parents and institutions when making decisions on behalf of children
Children of minor parents are under-represented in clinical trials. This is largely because of the e...
Background: Informed consent is an ethical practice that should be guaranteed before a child is invo...
Background: A challenge of performing research in the paediatric emergency and acute care setting is...
Part I of this Comment traces the development of ethical and legal guidelines for current informed c...
Since the mid- to late 1990s, the scientific and medical research community has sought to increase i...
© 2014 Dr. Nikola Aileen StepanovThe primary objectives of early phase clinical studies is to test n...
Bioethics guidelines vary in their response to children as research subjects. Children have been ig...
This paper briefly reviews highlights from decades of debates in medicine, law, bioethics, psycholog...
Because children are presumed to have insufficient cognitive ability to consent to participate in re...
Research with children involves more complex considerations with respect to assuring the voluntary p...
As pediatric biobank research grows, additional guidance will be needed about whether researchers sh...
markdownabstractPaediatric research ethics evolves around a central dilemma. Either one has to accep...
Increasingly, pleas are made for extending the involvement of minors in deci...
About the author: Maria Truong is a native of Wichita, Kansas. While at the School of Nursing she re...
Stringent rules concerning parental permission in some studies could be detrimental to adolescents. ...
Children of minor parents are under-represented in clinical trials. This is largely because of the e...
Background: Informed consent is an ethical practice that should be guaranteed before a child is invo...
Background: A challenge of performing research in the paediatric emergency and acute care setting is...
Part I of this Comment traces the development of ethical and legal guidelines for current informed c...
Since the mid- to late 1990s, the scientific and medical research community has sought to increase i...
© 2014 Dr. Nikola Aileen StepanovThe primary objectives of early phase clinical studies is to test n...
Bioethics guidelines vary in their response to children as research subjects. Children have been ig...
This paper briefly reviews highlights from decades of debates in medicine, law, bioethics, psycholog...
Because children are presumed to have insufficient cognitive ability to consent to participate in re...
Research with children involves more complex considerations with respect to assuring the voluntary p...
As pediatric biobank research grows, additional guidance will be needed about whether researchers sh...
markdownabstractPaediatric research ethics evolves around a central dilemma. Either one has to accep...
Increasingly, pleas are made for extending the involvement of minors in deci...
About the author: Maria Truong is a native of Wichita, Kansas. While at the School of Nursing she re...
Stringent rules concerning parental permission in some studies could be detrimental to adolescents. ...
Children of minor parents are under-represented in clinical trials. This is largely because of the e...
Background: Informed consent is an ethical practice that should be guaranteed before a child is invo...
Background: A challenge of performing research in the paediatric emergency and acute care setting is...