Use of Modafinil in the Treatment of Tinnitus

NCT ID: NCT00591019

Last Updated: 2015-10-08

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: PHASE1
• Total Enrollment: 7 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2006-08-31
• Study Completion Date: 2008-06-30

Brief Summary

A study on the effects of the FDA approved drug Modafinil upon attention problems associated with tinnitus. This is considered to be a safe drug with few side effects. Each subject will be asked to participate in 3 sessions each lasting approximately 1 hour in which cognitive testing and recordings will be taken. The study involves each subject taking a 2- week supply of Modafinil and a 2- week supply of placebo. We hypothesize inattention related to thalamocortical dysrhythmia found in tinnitus can be reduced by Modafinil thus improving vigilance.

Detailed Description

Modafinil, a drug primarily used in the treatment for narcolepsy, is also being using in treating attention problems found in Attention Deficit Hyperactive Disorder (ADHD). This study will investigate the efficacy of Modafinil upon attention deficits found in tinnitus patients by assessing pre-attentional and attentional processes (e.g., the amplitude of auditory evoked responses and simple reaction time).

Conditions

Tinnitus

Study Design

• Allocation Method: RANDOMIZED
• Primary Study Purpose: TREATMENT
• Blinding Strategy: SINGLE

Study Groups

modafinil

Group Type: ACTIVE_COMPARATOR

Modafinil

Intervention Type: DRUG

200 mg/day, morning dose

Placebo

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: OTHER

Sugar pill once per day in the morning.

Interventions

Modafinil

200 mg/day, morning dose

Intervention Type: DRUG

Placebo

Sugar pill once per day in the morning.

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

• The diagnosis of tinnitus should be established by subject through exam and history performed by study physician in Ear, Nose and Throat (ENT) clinic.
• Subjects will be age 20 or older.
• Subjects should have tinnitus symptoms severe enough to seek medical attention.
• Subjects will have been seen in the Hearing and Balance Center at University of Arkansas for Medical Sciences (UAMS).
• Subjects will have had an audiogram.
• Signed informed consent.
• Women of childbearing potential must have a negative pregnancy test at screening and before being prescribed the study drug.
• Peripheral neuropathy.
• Hematologic (minimal values) at screening Absolute neutrophil count > 1,500 mm^3 Hemoglobin > 8.0 g/dl Platelet count > 100,000 mm^3

Exclusion Criteria

Disease-Specific Concerns

• Subjects who have locally advanced breast cancer with skin ulceration will be excluded from this study due to the risk of worsening ulcers and healing difficulties
• Stage IV breast cancer
• Inflammatory breast cancer

General Medical Concerns

• Subjects with Echo Cardiogram performance status 2, 3, and 4 are not eligible for this study
• Allergy to any component of the treatment regimen
• Women who are breast feeding
• Pregnancy or refusal to use effective contraception while participating in this study
• Inability to comply with study and/or follow-up procedures
• Subjects with secondary malignancy other than superficial skin cancer (squamous cell carcinoma and basal cell carcinoma of the skin) should be excluded

Bevacizumab-Specific Concerns

• Current, recent (within 4 weeks of the first infusion of this study), or planned participation in an experimental drug study
• Blood pressure of > 150/100 mmHg. Essential hypertension well controlled with anti hypertensive is not an exclusion criterion
• Unstable angina
• New York Heart Association (NYHA) Grade II or greater congestive heart failure (see Appendix D)
• History of myocardial infarction within 6 months
• History of stroke within 6 months
• Clinically significant peripheral vascular disease
• Evidence of bleeding diathesis or coagulopathy
• Presence of central nervous system or brain metastases
• Major surgical procedure, open biopsy, or significant traumatic injury within 28 days prior to Day 0, anticipation of need for major surgical procedure during the course of the study
• Minor surgical procedures such as fine needle aspirations or core biopsies within 7 days prior to Day 0
• Pregnant (positive pregnancy test) or lactating
• Urine protein: creatinine ratio >1.0 at screening
• History of abdominal fistula, gastrointestinal perforation, or intra-abdominal abscess within 6 months prior to Day 0
• Serious, non-healing wound, ulcer, or bone fracture

• Minimum Eligible Age: 20 Years
• Maximum Eligible Age: 99 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

University of Arkansas

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

John L Dornhoffer, MD

Role: PRINCIPAL_INVESTIGATOR

University of Arkansas

Locations

University of Arkansas for Medical Sciences

Little Rock, Arkansas, United States

Countries

United States

Other Identifiers

# 65171

Identifier Type: -

Identifier Source: org_study_id