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Effect of Carbamazepine and Oxcarbazepine on Tinnitus

Evaluation of Carbamazepine and Oxcarbazepine effect on Tinnitus in patients referred to Amir Almomenin Hospital rasht-iran.

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT138903061138N2
Enrollment
57
Registered
2010-05-27
Start date
2010-08-21
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

nonpulsatile tinnitus. Other diseases of inner ear

Interventions

Intervention 1: Group A(carbamazepine): week 1 = tab 200 mg/daily week 2 -week 12= tab 600 mg/daily (300 mg/ BD). Intervention 2: Group b( oxcarbazepine ): week 1= 300 mg/daily then week2- week12 =
Treatment - Drugs
Placebo
Group A(carbamazepine): week 1 = tab 200 mg/daily week 2 -week 12= tab 600 mg/daily (300 mg/ BD)
Group b( oxcarbazepine ): week 1= 300 mg/daily then week2- week12 = 900 mg/ daily (450 mg BID)
Group C: intervention with placebo

Sponsors

Guilan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: 1-tinnitus history more than 6 months; 2- The patients 21-65 years with nonpulsatile tinnitus. Excllusion crateria:1-pulsatile tinnitus 2-mineare's disease 3-vestibular neurinoma 4-otosclerosis 5-the patients use of hearing-aid 6-pregnancy 7- patients with psychologic disorders need to treatment 8-the nontulerance minimal dose of carbamazepine and oxcarbazepine or hypersensitivity to these drugs 9-recent treatment with anti convulsion drugs 10-OCP consumptions and the drugs interaction with carbamazepine but are necessary to patients 10-patients with severe heart disease(CHF,IHD) 11- appearance severe drug hypersensitivity reaction during of treatment

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Tinnitus severity. Timepoint: The beginning of treatment and ending of 8th and 12th week. Method of measurement: VAS & TSI.;Quality of Life. Timepoint: The beginning of treatment and ending of 8th and 12th week. Method of measurement: TSI.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Houshang Gerami

Guilan University of Medical Sciences

gerami@gums.ac.ir+98 13 1222 5242

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026