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Clinical Trial Summary

The purpose of this study is to find out if continued monitoring of side effects from Selinexor and prescribed medication to prevent side effects helps improve symptoms, quality of life, and ability to continue the treatment longer.


Clinical Trial Description

The primary objective of this study is to evaluate control of treatment-related and cancer-associated symptoms over the first three months of therapy with selinexor in Veterans who participate in a telehealth symptom management intervention. The secondary objectives are: - To describe characteristics of patients treated with selinexor. - To describe adherence with the telehealth intervention. - To define the type and frequency of adverse events that patients experience while taking selinexor. - To describe the duration of selinexor therapy and evaluate adherence and dose intensity of selinexor in VA cancer patients receiving a telehealth symptom management intervention. - To describe concomitant medication usage in patients treated with selinexor. - To assess quality of life in patients treated with selinexor in the VA. - To estimate progression-free survival in VA cancer patients treated with selinexor. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06452446
Study type Observational
Source Durham VA Medical Center
Contact Daphne Friedman, MD
Phone (919) 286-0411
Email daphne.friedman@va.gov
Status Not yet recruiting
Phase
Start date July 1, 2024
Completion date July 1, 2028

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