Longitudinal Evaluation of Taxane Induced Neuropathy in Early Stage Breast Cancer

Status: Completed
Location: See location...
Study Type: Observational
SUMMARY

Longitudinal Evaluation of Taxane induced neuropathy in early stage breast cancer.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Patients (men and women) diagnosed with breast cancer stages I-III initiating first line adjuvant or neoadjuvant therapy with paclitaxel or docetaxel

• Ability to understand and the willingness to sign a written informed consent document.

• Patients with functional limitations due to musculoskeletal conditions can be included, because these conditions are known to remain stable over the relatively short duration of the study.

• Concurrent standard and investigational agents are permissible with the standard chemotherapy drugs.

Locations
United States
Ohio
Ohio State University Wexner Medical Center
Columbus
Time Frame
Start Date: 2013-12-04
Completion Date: 2018-05-14
Participants
Target number of participants: 62
Treatments
Breast cancer patients
This is a single arm study evaluating feasibility of evaluating gait and parameter changes in patients with early stage breast cancer undergoing adjuvant taxane chemotherapy.
Related Therapeutic Areas
Sponsors
Leads: Ohio State University Comprehensive Cancer Center

This content was sourced from clinicaltrials.gov

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