The main objective of this clinical trial placebo controled is to evaluate the action of intraauricular topical lidocaine on tinnitus. The question to be answered is whether lidocaine is superior to placebo (distilled water) in reducing tinnitus intensity when applied topically within the external auditory canal. Tinnitus intensity will be measured using the visual analog scale and acuphenometry before and after lidocaine or placebo application.
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Change in Visual Analogue Scale (VAS) Score
Timeframe: Immediately before and 5 minutes after receiving intervention on days 1 and 15
Change in Tinnitus Loudness
Timeframe: Immediately before and 5 minutes after receiving intervention on days 1 and 15
Change in Minimum Masking Level (MML)
Timeframe: Immediately before and 5 minutes after receiving intervention on days 1 and 15