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Clinical Trial Summary

To learn if a process called neuromodulation can help to improve pain due to CIP


Clinical Trial Description

Inclusion Criteria: - Ability to understand and the willingness to sign a written informed consent document - Patients diagnosed with CIPN lower extremity due to either vinca alkaloids, taxanes, bortezomib, thalidomide, platinum-based compounds - Patients seen at Pain Management Center at MD Anderson Cancer Center - Patient ages greater or equal to 18 years but less than or equal to 85 years Exclusion Criteria: - Patients with cognitive dysfunction - Patient with recent history (<6 months) of drug or alcohol abuse - Patients with open skin lesion or undergoing antibiotic therapy for local for systemic infection - Patients with painful diabetic peripheral neuropathy or preexisting peripheral neuropathy ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06121232
Study type Interventional
Source M.D. Anderson Cancer Center
Contact Saba Javed, M D
Phone (713) 792-9530
Email sjaved@mdanderson.org
Status Recruiting
Phase N/A
Start date November 2, 2023
Completion date April 1, 2026

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