Standardising management of consent withdrawal and other clinical trial participation changes: The UKCRC Registered Clinical Trials Unit Network's PeRSEVERE project.

Background/Aims: Existing regulatory and ethical guidance does not address real-life complexities in how clinical trial participants' level of participation may change. If these complexities are inappropriately managed, there may be negative consequences for trial participants and the integrity of t...

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Publicado en:	Clinical Trials Vol. 22; no. 5; pp. 578 - 597
Autores principales:	Cragg, William J, Clifton-Hadley, Laura, Dearling, Jeremy, Dutton, Susan J, Gillies, Katie, Hardy, Pollyanna, Hind, Daniel, Holm, Søren, Hood, Kerenza, Kearney, Anna, Lewis, Rebecca, Markham, Sarah, Moreau, Lauren, Pham, Tra My, Roberts, Amanda, Ruddock, Sharon, Sirovica, Mirjana, Sohanpal, Ratna, Tharmanathan, Puvan, Verghis, Rejina
Formato:	research tables/charts Journal Article
Publicado:	Sage Publications, Ltd. Oct2025
Acceso en línea:	Ver este registro en EBSCOhost