Efficacy and Safety of the Soricle for Subjective Tinnitus Relief

This study was conducted to evaluate the efficacy and safety of Soricle, a medical device combining transcutaneous vagus nerve stimulation and sound stimulation, in patients with subjective tinnitus. Participants were randomly assigned to either the active treatment group or a sham control group in a double-blind manner. The device was used daily for 8 weeks. The primary objective was to assess the improvement in tinnitus symptoms, and safety was evaluated throughout the study period.

NCT Number	NCT07548320
Lead Sponsor	Neurive Co.,Ltd.
Conditions	Tinnitus, Subjective Tinnitus
Enrollment	36 participants
Start Date	2025-03-10
Primary Completion	2025-09-08 (estimated)
Study Completion	2025-09-08 (estimated)
Updated on ClinicalTrials.gov	2026-04-23