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ePRO for the Timely Detection of Side Effects in Cancer Patients Undergoing CAR T Immunotherapy — CARTePRO  

Patient Reported Outcome Measures Clinical Trial

Official title:
ePRO for the Timely Detection of Side Effects in Cancer Patients Undergoing CAR T Immunotherapy: Feasibility Study (CARTePRO)

Clinical Trial Summary

This study is designed as a feasibility study implementing electronic Patient Reported Outcomes (ePRO) in CAR T treatment for hematological malignancies, in order to describe AE reporting. ePRO assessments will be explored for their feasibility to engage in monitoring and management of CAR T-related toxicities as well as using these digital ePRO tools may improve both, its safety and accessibility.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

  • Patient Reported Outcome Measures
Clinical Trial Details
NCT number NCT05354973
Study type Observational
Source Stiftung Swiss Tumor Institute
Contact Andreas Trojan, Prof.Dr.med
Phone +41 76 343 02 00
Email trojan@1st.ch
Status Recruiting
Phase
Start date March 21, 2022
Completion date April 30, 2025
View Details
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