Treatment Evaluation of Neuromodulation for Tinnitus - Stage A2

NACompletedINTERVENTIONAL
Enrollment

191

Participants

Timeline

Start Date

March 20, 2018

Primary Completion Date

October 2, 2018

Study Completion Date

July 18, 2019

Conditions
Tinnitus
Interventions
DEVICE

PS1-PS4

Participants in this arm shall be given PS1 during the first half of treatment and PS4 during the second half of treatment. During the expected 12-week treatment period, the participants will be presented with audio stimuli and electrical pulses for somatosensory stimulation.

DEVICE

PS6-PS10

Participants in this arm shall be given PS6 during the first half of treatment and PS10 during the second half of treatment. During the expected 12-week treatment period, the participants will be presented with audio stimuli and electrical pulses for somatosensory stimulation.

DEVICE

PS7-PS4

Participants in this arm shall be given PS7 during the first half of treatment and PS4 during the second half of treatment. During the expected 12-week treatment period, the participants will be presented with audio stimuli and electrical pulses for somatosensory stimulation.

DEVICE

PS9-PS6

Participants in this arm shall be given PS9 during the first half of treatment and PS6 during the second half of treatment. During the expected 12-week treatment period, the participants will be presented with audio stimuli and electrical pulses for somatosensory stimulation.

Trial Locations (1)

Unknown

St. James's Wellness Trust Clinical Research Facility, Dublin

Sponsors
All Listed Sponsors
lead

Neuromod Devices Ltd.

INDUSTRY

NCT03530306 - Treatment Evaluation of Neuromodulation for Tinnitus - Stage A2 | Biotech Hunter | Biotech Hunter