Patients With Subjective Tinnitus Clinical Trial
Official title:
Repetitive Transcranial Magnetic Stimulation (rTMS) Effect on Tinnitus
| NCT number | NCT02071732 |
| Other study ID # | 2014-002 |
| Secondary ID | |
| Status | Completed |
| Phase | N/A |
| First received | |
| Last updated | |
| Start date | February 2014 |
| Est. completion date | August 2021 |
| Verified date | August 2021 |
| Source | Dongtan Sacred Heart Hospital |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Interventional |
The purpose of this study is to determine whether repetitive transcranial magnetic stimulation (rTMS) is effective in the treatment of tinnitus.
| Status | Completed |
| Enrollment | 19 |
| Est. completion date | August 2021 |
| Est. primary completion date | August 2021 |
| Accepts healthy volunteers | No |
| Gender | All |
| Age group | 18 Years and older |
| Eligibility | Inclusion Criteria: - Subjective tinnitus - Age 18 years and older Exclusion Criteria: - Meniere, conductive hearing loss, objective tinnitus - History of seizure disorder or epilepsy - Clinically relevant psychiatric comorbidity - Previous symptomatic stroke - Surgically or traumatically implanted foreign bodies such as a pacemaker, an implanted medication pump, a metal plate in the skull, or metal inside the skull or eyes (other than dental appliances or fillings), intracardiac lines that may pose a physical hazard during magnetic stimulation |
| Country | Name | City | State |
|---|---|---|---|
| Korea, Republic of | Department of Neurology, and Department of Otorhinolaryngology-Head & Neck Surgery Dongtan Sacred Heart Hospital | Hwaseong-si | Gyeonggi-do |
| Lead Sponsor | Collaborator |
|---|---|
| Dongtan Sacred Heart Hospital |
Korea, Republic of,
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Tinnitus handicap inventory score | Primary outcomes will be measured twice. One is before, and the other is after 5-day rTMS interventions. Baseline primary outcome will be acceptable if it is done within the prior 6 months of 1st rTMS. Follow-up primary outcome will be done within the five days after 5th rTMS. | Before (- six months) and after (+ 5 days) rTMS interventions |