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Active Not RecruitingNCT01953159

Assessment of Paclitaxel-Induced Neuropathy

Validation of a Polygenic Neurotoxicity Risk Score in Patients With Unusually Severe Paclitaxel-Induced Neuropathy

Status
Active Not Recruiting
Phase
Study type
Observational
Enrollment
43 (actual)
Sponsor
University of Chicago · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Accepted

Summary

The purpose of this study is to collect clinical data, blood samples, and self reported symptoms from patients that experience unusually severe neuropathy after treatment with paclitaxel. This data will be used to develop predictive markers for neuropathy. Blood samples will be used to create induced pluripotent stem (iPS) cells and eventually artificial nerve cells to be used to study neuropathy in the lab.

Conditions

Interventions

TypeNameDescription
OTHERBlood Collection
OTHERPatient Questionnaires

Timeline

Start date
2013-08-29
Primary completion
2027-05-19
Completion
2027-12-01
First posted
2013-09-30
Last updated
2025-06-08

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01953159. Inclusion in this directory is not an endorsement.

Assessment of Paclitaxel-Induced Neuropathy (NCT01953159) · Clinical Trials Directory