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Study identifier: NCT07596030 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Self-applied taVNS for CIPN

Condition: Chemotherapy Induced Peripheral Neuropathy  ·  Sponsor: University of Miami

PhaseNA
Planned participants36
Who can joinAll sexes, 18 Years to 80 Years
Healthy volunteersNo

About this study

The purpose of this study is to determine the feasibility of using a portable device at home to self-administer transcutaneous auricular vagus nerve stimulation (taVNS). This handheld device has two small electrodes that are placed on specific areas of the outer ear. This device delivers a mild electrical stimulation to the vagus nerve through the ear. This study will explore how taVNS may affect symptoms of chemotherapy-induced peripheral neuropathy (CIPN). Participants will be assigned to one of two cohorts based on the presence of chemotherapy-induced peripheral neuropathy (CIPN). Participants with CIPN will be placed in the intervention cohort (n=24) and will complete a 2-week trial of daily self-applied taVNS. Participants without CIPN will be placed in the registry cohort (n=12) and will complete study measurements without receiving the intervention. The registry cohort will not receive the taVNS intervention but will undergo identical physiological assessments at baseline and at a 2 week follow up to control for testing effects and biological variability.

This description comes directly from the study's public registry record.

Talk to the study team

Richard L Martinez, MSPH  ·  3052842359  ·  rxm1388@med.miami.edu

Marlon L Wong, PT, PhD  ·  3052842670  ·  mwong2@miami.edu

Always discuss trial participation with your own doctor first.

Locations (1)

University of Miami, Plumer BuildingCoral Gables, Florida, United StatesRecruiting

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Source record: clinicaltrials.gov/study/NCT07596030