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Clinical Trial Summary

In this study, the investigators obtain wearable disease based biomarkers from patients diagnosed with cancer and undergoing chemotherapy, and simultaneously measure patient self-reported adverse events through an app to evaluate chemotherapy completion rates, emergency room visits, and frequency of CTCAE adverse events. The investigators will develop an artificial intelligence-based algorism that can predict patients' side effects based on biomarkers alone.


Clinical Trial Description

In this study, patients diagnosed with lung, head and neck, and esophageal cancers and undergoing chemotherapy will be measured for self-reported side effects using a wearable device to collect biomarkers through an app, and the association between patient quality of life and side effects and biomarkers obtained from the wearable device will be analyzed. On the other hand, blood (EDTA 3cc) for pharmacogenomics testing will be tested once at any point during the study period as an indicator associated with side effects after chemotherapy. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05937477
Study type Observational [Patient Registry]
Source Samsung Medical Center
Contact Sehhoon Park, MD
Phone +82-10-9185-8619
Email sehhoon.park@samsung.com
Status Recruiting
Phase
Start date June 8, 2023
Completion date June 30, 2026

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