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Clinical Trial Summary

The aim of this study is to determine whether the use of breast cancer patients' own electronic reporting of side effects to chemotherapy in a treatment setting has an impact on the handling of side effects and on the number of hospitalizations, febrile neutropenia and dose adjustments. We are using the Patient-Reported Outcomes version of the Common Terminology Criteria for Adverse Events (PRO-CTCAE) for the patients' reporting of side effects.

Clinical Trial Description


Study Design

Related Conditions & MeSH terms

NCT number NCT02996201
Study type Interventional
Source Rigshospitalet, Denmark
Status Completed
Phase N/A
Start date November 2015
Completion date January 2017

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