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Enhancing randomized clinical trials with digital twins
8
Zitationen
11
Autoren
2025
Jahr
Abstract
Digital twins (DTs) can transform randomized clinical trials by improving ethical standards, including safety, informed consent, equity, and data privacy. They also enhance trial efficiency by enabling early detection of adverse events and streamlined design. This paper explores the role of DTs in personalized medicine, from pre-clinical research to post-marketing, while addressing technological, legal, and ethical challenges in implementation.
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Autoren
Institutionen
- Washington University in St. Louis(US)
- University of Utah(US)
- Missouri Baptist Medical Center(US)
- UNSW Sydney(AU)
- St George Hospital(AU)
- The University of Melbourne(AU)
- Shahid Beheshti University of Medical Sciences(IR)
- Webster University(US)
- Shahed University(IR)
- Broad Institute(US)
- Brigham and Women's Hospital(US)
- Harvard University(US)
- Texas Tech University(US)
- Texas Tech University Health Sciences Center(US)
- Yale University(US)
- University School(US)
- Case Western Reserve University(US)