In medical research, the patient must be informed that the procedure is experimental and that consent can be withdrawn at any time. In addition, the person signing the consent form must be informed of the risks and benefits of the experimental procedure and of alternative treatments. Miller-...
Centre for Ageing Research and Education, Duke-NUS Medical School, Singapore, Singapore Rahul Malhotra HCA Hospice Limited, Singapore, Singapore Poh Heng Chong Department of Neonatology, Khoo Tech Puat-National University Children’s Medical Institute, National University Hospital, Singapore, Singapore Zuba...
All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional research committee and with the 1964 Helsinki declaration and its later amendments or comparable ethical standards. Informed consent Informed consent was obtained from all partic...
In conclusion, we have shown through our data that gold standards set by the Children's Act 1989 are met in our everyday clinical practice. Only legal guardians signed the consent form for the children. This study is a useful method to quantify our practice and maintain the delivery of high...
President Clinton yesterday seemingly supported both sides in the abortion debate but ensured that "partial-birth" abortion, a late-term procedure that Congress has sought to ban, will remain available as a form of birth control. P Bedard 被引量: 0发表: 0年 ...
The project was approved by the Ethics Committee of Beijing Anding Hospital (201743FS-2) and performed in accordance with the ethical standards laid down in the 1964 Declaration of Helsinki and its later amendments. All subjects and their parents signed an informed consent form before joining the...
In the UK, the Central Office for Research Ethics Committees considered that there is a profound difference between accessing medical interventions and participating in research. This organization argues that parental consent is an ethical, if not a legal, requirement prior to the involvement of ...
Data were collected through unstructured and semi-structured interviews, observations, psychological tests (Rorschach test for the parents and Blacky test for the child), and analysis of documented evidence that was presented in the trial. Written consent was obtained from the parents. ...
Printed informed consent forms and questionnaires were uniformly distributed by research assistants. After reading the informed consent form and fully understanding the purpose and risks of participating in the study, students voluntarily completed the questionnaire anonymously. They could withdraw from the ...
As participants had self-selected into the parent study, they may have had a more positive view of health research or might have also wanted additional contact with the medical sys- tem which could bias them towards consenting. We identified very few factors significantly associated with consent,...