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Objective Evaluation of Paclitaxel/Docetaxel-induced Neuropathy in Breast Cancer Patients

Breast Cancer Clinical Trial

Official title:
Objective Evaluation of Paclitaxel/Docetaxel-induced Neuropathy in Breast Cancer Patients

Clinical Trial Summary

The purpose of this prospective, non-interventional study is to perform neurological and cognitive assessment of breast cancer patients who receive standard of care single agent weekly paclitaxel docetaxel chemotherapy to determine the onset and severity of chemotherapy induced neuropathy (CIPN) and cognitive impairment (CICI).

Clinical Trial Description

The purpose of this prospective, non-interventional study is to perform neurological and cognitive assessment of breast cancer patients who receive standard of care single agent weekly paclitaxel or docetaxel chemotherapy to determine the onset and severity of chemotherapy induced neuropathy (CIPN) and cognitive impairment (CICI). ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03872141
Study type Observational
Source Yale University
Contact
Status Completed
Phase
Start date May 23, 2017
Completion date February 25, 2021
View Details
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