Cargando…
1065. Patient-Reported Reasons for Non-Participation in Inpatient COVID-19 Clinical Research: Results from a Multi-Center VA Embedded Randomized Trial
BACKGROUND: Early in the COVID-19 pandemic, no evidence-proven therapeutics were approved, and thus participation in a clinical trial was often the only way to access experimental medications. However, in the US, participation in medical research is low. Patient-stated factors impacting enrollment d...
Autores principales: | Reyes Dassum, Samira, Ferguson, Ryan, Woods, Patricia, Flynn, Maura, Visnaw, Karen, Schiller, Sara J, Monach, Paul, Leatherman, Sarah, Branch-Elliman, Westyn |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9752147/ http://dx.doi.org/10.1093/ofid/ofac492.906 |
Ejemplares similares
-
Patient- reported reasons for non-participation in a COVID-19 therapeutics clinical trial: Findings from a multi-center investigation
por: Dassum, Samira Reyes, et al.
Publicado: (2023) -
Implementation of documented and written informed consent for clinical trials of communicable diseases: Lessons learned, barriers, solutions, future directions identified during the conduct of a COVID-19 clinical trial
por: Woods, Patricia, et al.
Publicado: (2021) -
517. Subcutaneous Sarilumab for the Treatment of Hospitalized patients with Moderate to Severe COVID19 Disease: A Pragmatic, Embedded, Multi-Center Randomized Clinical Trial
por: Branch-Elliman, Westyn, et al.
Publicado: (2021) -
Subcutaneous sarilumab for the treatment of hospitalized patients with moderate to severe COVID19 disease: A pragmatic, embedded randomized clinical trial
por: Branch-Elliman, Westyn, et al.
Publicado: (2022) -
Reconsidering ‘minimal risk’ to expand the repertoire of trials with waiver of informed consent for research
por: Monach, Paul A, et al.
Publicado: (2021)