Health Condition 1: H931- Tinnitus
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Patients with perceived tinnitus for a minimum duration of 3 months and Willing to give written consent and take part in the study
Exclusion criteria
Exclusion criteria: 1.) Patient refusal 2.) Patients who have any internal electrical device (example: cardiac pacemakers and metal plates) 3.) Patients having pre-existing cardiac disorders . 4.) Cases of objective tinnitus ( eg . glomus tumour , palatal myoclonus ) 5.) If they had received TENS, acupuncture, or electroacupuncture for any other condition 6.) Pregnancy
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To study reduction in subjective sensation in tinnitus using Tinnitus Handicap Inventory , Visual Analogue ScaleTimepoint: To study reduction in subjective sensation in tinnitus using Tinnitus Handicap Inventory , Visual Analogue Scale at end of each session that will be undertaken twice a week for 4 weeks and thereafter at 1 month , 3 months and 6 months | — |
Secondary
| Measure | Time frame |
|---|---|
| To estimate the severity of tinnitus as assessed by Tinnitus handicap index. To study the duration of effect of TENS , on tinnitus. To determine the effect of transcutaneous electrical nerve stimulation on various domains of THI . Timepoint: To estimate the severity of tinnitus, duration of reduction in subjective sensation of tinnitus if any ,to determine the effect of transcutaneous electrical nerve stimulation on various domains of THI using Tinnitus Handicap Inventory , Visual Analogue Scale at end of each session that will be undertaken twice a week for 4 weeks and thereafter at 1 month , 3 months and 6 months | — |
Countries
India
Contacts
AIIMS Mangalagiri