Cargando…
Protecting Vulnerable Research Subjects in Critical Care Trials: Enhancing the Informed Consent Process and Recommendations for Safeguards
Although critically ill patients represent a vulnerable group of individuals, guidelines in research ethics assert that ethically acceptable research may proceed with such vulnerable subjects if additional safeguards are in place to minimize the risk of harm and exploitation. Such safeguards include...
Autor principal: | Silverman, Henry |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3224458/ https://www.ncbi.nlm.nih.gov/pubmed/21906335 http://dx.doi.org/10.1186/2110-5820-1-8 |
Ejemplares similares
-
Safeguarding vulnerable patients
por: Ide, Sarah
Publicado: (2021) -
From ‘Consent or Anonymise’ to ‘Share and Protect’: Facilitating Access to Surplus Tissue for Research Whilst Safeguarding Donor Interests
por: Blewett, Catherine
Publicado: (2021) -
Aspects of vulnerable patients and informed consent in clinical trials
por: Kuthning, Maria, et al.
Publicado: (2013) -
A review of informed consent and how it has evolved to protect vulnerable participants in emergency care research
por: Nandra, Rajpal, et al.
Publicado: (2020) -
Consenting of the vulnerable: the informed consent procedure in advanced cancer patients in Mexico
por: Verástegui, Emma L
Publicado: (2006)