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Clinical Trial Summary

Despite enormous advances in thoracic surgery and oncology, two critical issues concern patients undergoing curative-intent surgery for lung, gastric and esophageal cancer: first, a majority (~60%) of patients experience minor and major adverse events occurring during and in the days following surgery; second, patients worry about the significant risk of cancer recurrence and mortality months to years after surgery. These issues, combined with side effects of chemotherapy and radiation, have detrimental effects on health-related quality of life (HRQoL). On a deeper level, there is the problem of an ongoing failure to integrate and evaluate the best of what complementary medicine has to offer surgical oncology care. Too many clinical trials focus on single agent therapies, rather than broad multi-faceted individualized and integrative care interventions that are used in real world settings. The Thoracic POISE project has the overarching goal of improving care for thoracic cancer patients by impacting HRQoL, reducing surgical adverse events, prolonging overall survival and pioneering integrative care delivery.


Clinical Trial Description

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Study Design


Related Conditions & MeSH terms


NCT number NCT04871412
Study type Interventional
Source Ottawa Hospital Research Institute
Contact Anna Fazekas, MA, CCRP
Phone 613-737-8899
Email afazekas@toh.ca
Status Recruiting
Phase Phase 3
Start date April 4, 2022
Completion date December 1, 2025

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