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Influence of Tonic and Burst Transcranial Magnetic Stimulation (TMS) Characteristics on Acute Inhibition of Subjective Tinnitus

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ClinicalTrials.gov Identifier: NCT00878696
Recruitment Status : Completed
First Posted : April 9, 2009
Last Update Posted : April 9, 2009
Sponsor:
Information provided by:

Study Description
Brief Summary:
Transcranial magnetic stimulation (TMS) is already broadly used in different areas of neuroscience research. Last year, special attention was drawn to TMS in tinnitus. The aim of the researchers' study is to investigate the stimulation characteristics of TMS in tinnitus patients, in particularly the effect of tonic and burst stimulation of the superior temporal lobe.

Condition or disease Intervention/treatment
Tinnitus Procedure: TMS transcranial magnetic stimulation

Study Design

Study Type : Observational
Actual Enrollment : 64 participants
Observational Model: Case-Only
Time Perspective: Retrospective
Official Title: Influence of Tonic and Burst TMS Characteristics on Acute Inhibition of Subjective Tinnitus
Study Start Date : January 2007
Primary Completion Date : September 2007
Study Completion Date : April 2008

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Tinnitus
U.S. FDA Resources

Groups and Cohorts

Group/Cohort Intervention/treatment
Tinnitus
Tinnitus patients
Procedure: TMS transcranial magnetic stimulation

200 pulses of tonic TMS (see Graph 1) were administered with an intensity at 50% of the maximal TMS device output (50%DO).

The frequency of the tonic pulses was randomly chosen between 1Hz, 5Hz, 10Hz or 20Hz.

Burst stimulation was delivered at a burst frequency of 5, 10 or 20Hz. Each burst consisted of 3, 5 or 10 pulses. The individual pulse rate within a burst was 50 or 100Hz.



Outcome Measures

Primary Outcome Measures :
  1. VAS visual analogue scale [ Time Frame: immediately before and immediately after single session TMS ]

Eligibility Criteria

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 78 Years   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population
Patients presented to our Multidisciplinary Tinnitus Clinic with tinnitus as a main complaint.
Criteria

Inclusion Criteria:

  • Patients presented to our Multidisciplinary Tinnitus Clinic with tinnitus as a main complaint.

Exclusion Criteria:

  • Patients with known history of epilepsy, pacemakers, cochlear implants, neurostimulators or intracerebral pathology were excluded from the study.
Contacts and Locations

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00878696


Locations
Belgium
Antwerp University Hospital
Edegem, Antwerp, Belgium, 2650
Sponsors and Collaborators
University Hospital, Antwerp
More Information

Responsible Party: Prof Van de Heyning, UZA
ClinicalTrials.gov Identifier: NCT00878696     History of Changes
Other Study ID Numbers: ITBTMS
First Posted: April 9, 2009    Key Record Dates
Last Update Posted: April 9, 2009
Last Verified: April 2009

Additional relevant MeSH terms:
Tinnitus
Hearing Disorders
Ear Diseases
Otorhinolaryngologic Diseases
Sensation Disorders
Neurologic Manifestations
Nervous System Diseases
Signs and Symptoms