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Clinical Trial Summary

This study investigates the use of digital and standardized documentation by patients of frequently occurring adverse events in oncological therapies.


Clinical Trial Description

This research study is structured as a Phase I and II clinical trial. In phase I, the feasibility of using a smartphone application to document adverse events that have occurred during oncological therapies by the patient will be investigated. In phase II we will investigate whether the use of the smartphone app allows an improvement of patient care by reducing occurred adverse events. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04493450
Study type Observational [Patient Registry]
Source University of Ulm
Contact Thomas Seufferlein, Prof. Dr.
Phone +4973150044501
Email thomas.seufferlein@uniklinik-ulm.de
Status Not yet recruiting
Phase
Start date September 1, 2020
Completion date June 30, 2022

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