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Ensayo clínico

Efficacy and Safety of the Soricle for Subjective Tinnitus Relief

NCT: NCT07548320 · COMPLETED

ID NCTNCT07548320
EstadoCOMPLETED
Fecha de inicio2025-03-10
Finalización2025-09-08

Resumen breve

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.

Fuente oficial

Ver en ClinicalTrials.gov →

Datos obtenidos de la API de ClinicalTrials.gov. Para conocer el estado más reciente, consulte el registro oficial.

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