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Repetitive Transcranial Magnetic Stimulation for Chronic Subjective Tinnitus

Primary Purpose

Tinnitus, Subjective

Status
Completed
Phase
Not Applicable
Locations
Czechia
Study Type
Interventional
Intervention
Repetitive Transcranial Magnetic Stimulation
Sham stimulation
Ginkgo Biloba Extract
Sponsored by
University Hospital Ostrava
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Tinnitus, Subjective focused on measuring chronic tinnitus, repetitive transcranial magnetic stimulation, hypacusion, depression, treatment, placebo, medication therapy

Eligibility Criteria

18 Years - 99 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

- subjective chronic non-pulsatile tinnitus lasting more than 6 months

Exclusion Criteria:

  • head injury or brain surgery
  • epilepsy
  • organic brain lesion
  • Meniere's disease or fluctuating hearing loss
  • cochlear or bone-anchored hearing device implantation
  • history of suicide
  • pregnancy
  • therapy with anticonvulsants
  • antipsychotic medication
  • heart pacemaker implantation
  • rTMS performed in the past
  • not signing of the informed consent

Sites / Locations

  • University Hospital Ostrava

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Sham Comparator

Active Comparator

Arm Label

Repetitive Transcranial Magnetic Stimulation

Sham stimulation

Ginkgo Biloba Extract

Arm Description

Patients in this study arm will undergo the rTMS stimulation as described above.

Patients in this study arm will undergo the sham stimulation as described above.

Patients in this study arm will receive medication therapy as described above, without any rTMS or sham procedure.

Outcomes

Primary Outcome Measures

Tinnitus Reaction Questionnaire (TRQ)
This questionnaire will be used to find out what sort of effects tinnitus has had on the lifestyle and general well-being of the patients. 10% improvement will be considered clinically relevant.
Tinnitus Handicap Questionnaire (THQ)
This questionnaire has 27 questions and will be used to assess the degree of handicap that the tinnitus presents for the affected patients. 10% improvement will be considered clinically relevant.
Tinnitus Handicap Inventory (THI)
The purpose of this questionnaire is to identify difficulties the affected patients may be experiencing because of tinnitus. 10% improvement of the score will be considered clinically relevant.

Secondary Outcome Measures

Improvement of depression - Beck Depression Inventory
Improvement of depressive symptoms in patients will be assessed using the Beck Depression Inventory (BDI) test.
Improvement of hearing loss - Fowler scoring
Improvement of the hearing loss in patients will be assessed using the pure-tone audiometry with Fowler scoring of hearing loss (%).

Full Information

First Posted
January 15, 2018
Last Updated
June 1, 2018
Sponsor
University Hospital Ostrava
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1. Study Identification

Unique Protocol Identification Number
NCT03425045
Brief Title
Repetitive Transcranial Magnetic Stimulation for Chronic Subjective Tinnitus
Official Title
Repetitive Transcranial Magnetic Stimulation for Chronic Subjective Non-Pulsatile Primary Tinnitus Compared to Placebo and Medicament Therapy
Study Type
Interventional

2. Study Status

Record Verification Date
June 2018
Overall Recruitment Status
Completed
Study Start Date
March 1, 2015 (Actual)
Primary Completion Date
March 31, 2018 (Actual)
Study Completion Date
March 31, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital Ostrava

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Therapy of subjective chronic primary tinnitus could be challenging. Repetitive transcranial magnetic stimulation (rTMS) is currently being tested for suppressing the symptoms. However, effect of stimulation remains controversial. The aim was to uncover real effect of rTMS stimulation for tinnitus treatment. There will be three groups, stimulation group, sham stimulation group and controlled group with medicament treatment. The investigators assume that combination of rTMS stimulation of dorsolateral prefrontal cortex and primary auditory cortex at both sides will be more efficient. The investigators considered a 10% improvement in the tinnitus questionnaire score and in the tinnitus masking to be clinically relevant.
Detailed Description
Adult patients suffering from chronic subjective non-pulsatile primary unilateral or bilateral tinnitus for at least 6 months will be included in the study. Patients will be randomly assigned using a random number generation randomization method into rTMS stimulation group (group 1), sham stimulation group (group 2) and group with medicament therapy only (group 3). Dorsolateral prefrontal cortex (frequency 25 Hz; 300 pulses; 80% resting motor threshold=RMT) and primary auditory cortex on both sides (1 Hz; 1000 pulses; 110% RMT) will be stimulated in patients in rTMS stimulation group for 5 consecutive days. Both the patients and outcome assessor were blinded to the intervention group in which the patients (rTMS and shame stimulation group) belonged to. Medicament therapy in group 3 will consist of ginkgo biloba extract EGb 761 once a day for 6 months. There will be no medicament therapy for tinnitus in group 1 and 2. Tinnitus reaction questionnaire (TRQ), tinnitus handicap questionnaire (THQ), tinnitus handicap inventory (THI), Beck Depression Inventory (BDI), pure-tone audiometry with Fowler scoring of hearing loss and tinnitus analysis will be used for evaluation of tinnitus in all patients. Data will be recorded on the day patient is included in the study, during follow-up after 1 month and 6 months. Descriptive statistics, such as the arithmetic mean, standard deviation, and absolute and relative frequency tables, will be used for data processing. The Pearson's chi-squared test, Fisher's exact test, Kruskal-Wallis test and analysis of variance will be used for comparison. The statistical tests will be assessed using a significance level of 5%.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Tinnitus, Subjective
Keywords
chronic tinnitus, repetitive transcranial magnetic stimulation, hypacusion, depression, treatment, placebo, medication therapy

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
The study is designed as interventional, blinded, randomized, controlled trial with three parallel arms
Masking
ParticipantOutcomes Assessor
Masking Description
The study subjects and outcomes assessors will be masked, the investigator will know which treatment is being provided for which patient.
Allocation
Randomized
Enrollment
40 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Repetitive Transcranial Magnetic Stimulation
Arm Type
Experimental
Arm Description
Patients in this study arm will undergo the rTMS stimulation as described above.
Arm Title
Sham stimulation
Arm Type
Sham Comparator
Arm Description
Patients in this study arm will undergo the sham stimulation as described above.
Arm Title
Ginkgo Biloba Extract
Arm Type
Active Comparator
Arm Description
Patients in this study arm will receive medication therapy as described above, without any rTMS or sham procedure.
Intervention Type
Procedure
Intervention Name(s)
Repetitive Transcranial Magnetic Stimulation
Intervention Description
Patients randomised in Arm 1 will receive stimulation of the dorsolateral prefrontal cortex (frequency 25 Hz; 300 pulses; 80% resting motor threshold=RMT) and primary auditory cortex on both sides (1 Hz; 1000 pulses; 110% RMT) will be stimulated in patients in rTMS stimulation group for 5 consecutive days. No medication therapy will be provided for patients in this arm.
Intervention Type
Procedure
Intervention Name(s)
Sham stimulation
Intervention Description
Sham stimulation will be performed in patients randomised in Arm 2 of the study for 5 consecutive days. No medication therapy will be provided for patients in this arm.
Intervention Type
Drug
Intervention Name(s)
Ginkgo Biloba Extract
Intervention Description
Patients randomised in Arm 3 of the study will receive medication therapy with Ginkgo biloba extract EGb 761 once a day for 6 months.
Primary Outcome Measure Information:
Title
Tinnitus Reaction Questionnaire (TRQ)
Description
This questionnaire will be used to find out what sort of effects tinnitus has had on the lifestyle and general well-being of the patients. 10% improvement will be considered clinically relevant.
Time Frame
36 months
Title
Tinnitus Handicap Questionnaire (THQ)
Description
This questionnaire has 27 questions and will be used to assess the degree of handicap that the tinnitus presents for the affected patients. 10% improvement will be considered clinically relevant.
Time Frame
36 months
Title
Tinnitus Handicap Inventory (THI)
Description
The purpose of this questionnaire is to identify difficulties the affected patients may be experiencing because of tinnitus. 10% improvement of the score will be considered clinically relevant.
Time Frame
36 months
Secondary Outcome Measure Information:
Title
Improvement of depression - Beck Depression Inventory
Description
Improvement of depressive symptoms in patients will be assessed using the Beck Depression Inventory (BDI) test.
Time Frame
36 months
Title
Improvement of hearing loss - Fowler scoring
Description
Improvement of the hearing loss in patients will be assessed using the pure-tone audiometry with Fowler scoring of hearing loss (%).
Time Frame
36 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
99 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: - subjective chronic non-pulsatile tinnitus lasting more than 6 months Exclusion Criteria: head injury or brain surgery epilepsy organic brain lesion Meniere's disease or fluctuating hearing loss cochlear or bone-anchored hearing device implantation history of suicide pregnancy therapy with anticonvulsants antipsychotic medication heart pacemaker implantation rTMS performed in the past not signing of the informed consent
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Michal Bar, Ass.Prof.,MD,PhD
Organizational Affiliation
University Hospital Ostrava
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Hospital Ostrava
City
Ostrava
State/Province
Moravian-Silesian Region
ZIP/Postal Code
70852
Country
Czechia

12. IPD Sharing Statement

Plan to Share IPD
Undecided
IPD Sharing Plan Description
The plan to share IPD to other researchers has not been decided yet.
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Links:
URL
http://www.audiology.org
Description
The American Academy of Audiology is the world's largest professional organization of, by, and for audiologists.
URL
http://www.hear-it.org
Description
The world's #1 website on hearing and hearing loss, since 1999.

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Repetitive Transcranial Magnetic Stimulation for Chronic Subjective Tinnitus

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