Selected article for: "clinical trial and sample size"

Author: Malfettone, Andrea; Di Cosimo, Serena; Pérez-García, José Manuel; García, Alicia; Sampayo-Cordero, Miguel; Mina, Leonardo; Herrero, Carolina; Llombart-Cussac, Antonio; Cortés, Javier
Title: Nobody dares stopping clinical research, not even COVID-19
  • Cord-id: 0n24qglq
  • Document date: 2021_4_8
  • ID: 0n24qglq
    Snippet: In the global health emergency caused by the COVID-19, clinical trial management has proven to be critical for the pharmaceutical industry, sponsors, and healthcare professionals. Our experience as a sponsor managing interventional oncology clinical studies has provided us with some data and insights. Though limited by sample size, our data emphasize the importance of quickly adopting measures that first prioritize patient safety and data validity, then consider contingency measures such as tele
    Document: In the global health emergency caused by the COVID-19, clinical trial management has proven to be critical for the pharmaceutical industry, sponsors, and healthcare professionals. Our experience as a sponsor managing interventional oncology clinical studies has provided us with some data and insights. Though limited by sample size, our data emphasize the importance of quickly adopting measures that first prioritize patient safety and data validity, then consider contingency measures such as telemedicine, virtual medical review, and remote monitoring. Successful adaptations of healthcare and patient management in response to COVID-19 have been fundamental to ensuring continuing clinical cancer research.

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