- Open Access
- Article
The Dual Impact of AI in Clinical Trials: Perspective
by Muhammad Yaqub 1 and Lan He 1
1 School of Biomedical Sciences, Hunan University, Changsha, 410000, P.R China
* Author to whom correspondence should be addressed.
Journal of Engineering Research and Sciences, Volume 3, Issue 9, Page # 16-25, 2024; DOI: 10.55708/js0309002
Keywords: Artificial Intelligence, Clinical Trials, Patient Outcomes, Predictive Analytics, Healthcare Inequities
Received: 07 August 2024, Revised: 05 September 2024, Accepted: 02 March 2023, Published Online: 30 January 2024
(This article belongs to the Special Issue Special Issue on Multidisciplinary Sciences and Advanced Technology 2024 & Section Biochemical Research Methods (BRM))
APA Style
Yaqub, M., & He, L. (2024). The dual impact of AI in clinical trials: Perspective. Journal of Engineering Research and Sciences, 3(9), 16-25. https://doi.org/10.55708/js0309002
Chicago/Turabian Style
Yaqub, Muhammad, and Lan He. “The Dual Impact of AI in Clinical Trials: Perspective.” Journal of Engineering Research and Sciences 3, no. 9 (2024): 16-25. https://doi.org/10.55708/js0309002.
IEEE Style
M. Yaqub and L. He, “The Dual Impact of AI in Clinical Trials: Perspective,” Journal of Engineering Research and Sciences, vol. 3, no. 9, pp. 16-25, 2024, doi: 10.55708/js0309002.
The use of artificial intelligence in clinical trials opens the way for a period of transformation in which the potential to enhance efficiency, precision, and scope in clinical investigation is enormous. In this perspective, the promise and perils of AI regarding clinical trials are critically reviewed. On one hand, it’s where AI can really make some revolutionary changes to the most critical aspects of trial design and execution—like patient recruitment, data management, and predictive analytics—which are now adaptive and more driven by data; on the other hand, AI applied in clinical trials also brings considerable problems related to data integrity, ethical considerations, and regulatory compliance. Such potential of AI to further biases, break patient confidences, and exacerbate already wide inequities in healthcare raises the need for vigilant oversight. As AI is rapidly evolving, so too are principles that guide transparency, fairness, and ethical rigors that guide their application in clinical trials. This work presents a case for strong AI frameworks that are subject to firm validation and ethical scrutiny, which will ensure that the benefits of AI are realized with reduced risks associated with it. If the field goes down this road, AI integration in clinical trials is going to be the real catalyst for innovation, which could translate into achieving better patient outcomes and expanding frontiers for medical science.
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