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Dose finding of tocainide in the treatment of tinnitus

International Journal of Clinical Pharmacology, Therapy, and Toxicology
|April 1, 1986
PubMed

Insights

Oral tocainide showed symptom regression in some tinnitus patients at higher doses. However, frequent side effects, including rash, limit its use and it is not a satisfactory alternative to intravenous lidocaine.

Area of Science:

  • Pharmacology
  • Otolaryngology

Background:

  • Tinnitus is a common auditory condition affecting millions.
  • Limited effective oral treatments for tinnitus exist, necessitating research into novel therapeutic agents.

Purpose of the Study:

  • To determine the optimal and safe dosage of oral tocainide for tinnitus management.
  • To evaluate the efficacy and tolerability of tocainide in a dose-finding study for tinnitus.

Main Methods:

  • A single-blind, dose-escalation study involving 19 tinnitus patients.
  • Administration of oral tocainide hydrochloride in doses from 0 to 1800 mg, with effects and serum concentrations monitored.
  • Each dose was administered for four days.

Main Results:

  • Symptom reduction to a non-troublesome level was observed in 8 out of 19 patients, primarily at 900 mg and 1800 mg doses.
  • Frequent side effects were noted, with a significant incidence of exanthema (37% of patients).
  • The therapeutic benefit of tocainide was deemed low compared to intravenous lidocaine.

Conclusions:

  • A daily dose of oral tocainide exceeding 900 mg is not justified for tinnitus treatment due to side effect profile.
  • Tocainide is not considered a satisfactory alternative to intravenous lidocaine for tinnitus management.

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