Actively Recruiting

Phase Not Applicable
Age: 18Years - 85Years
All Genders
NCT06162403

Exploring the Benefit of Peripheral Nerve Stimulation in Treating Pain From Chemo-induced Peripheral Neuropathy: A Longitudinal Single Center Feasibility Study

Led by M.D. Anderson Cancer Center · Updated on 2026-02-19

10

Participants Needed

1

Research Sites

201 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

To learn if peripheral nerve stimulation (PNS) can help to improve pain in participants with CIPN.

CONDITIONS

Official Title

Exploring the Benefit of Peripheral Nerve Stimulation in Treating Pain From Chemo-induced Peripheral Neuropathy: A Longitudinal Single Center Feasibility Study

Who Can Participate

Age: 18Years - 85Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Participants diagnosed with chronic (≥90 days duration) chemotherapy-induced peripheral neuropathy of the lower extremity
  • Participants report baseline pain score of 4 or higher on a 0-10 scale
  • Participants aged between 18 and 85 years old
  • Participants who completed chemotherapy within the previous year at enrollment
Not Eligible

You will not qualify if you...

  • Participants with cognitive dysfunction
  • Participants with drug or alcohol abuse history within the past 6 months
  • Participants with open skin lesions or receiving antibiotic treatment for infection
  • Participants allergic to local anesthesia, steroids, or adhesives
  • Participants with conditions conflicting with the SPRINT PNS System contraindications and warnings

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

MD Anderson Cancer Center

Houston, Texas, United States, 77030

Actively Recruiting

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Research Team

S

Saba Javed, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

SUPPORTIVE_CARE

Number of Arms

1

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