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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00833950
Other study ID # 8/2/12
Secondary ID
Status Completed
Phase Phase 4
First received January 30, 2009
Last updated March 2, 2009
Start date March 2008

Study information

Verified date December 2008
Source University Hospital, Antwerp
Contact n/a
Is FDA regulated No
Health authority Belgium: Federal Agency for Medicinal Products and Health Products
Study type Interventional

Clinical Trial Summary

Phase shift treatment is a new tinnitus therapy that aims at sound cancelling via complete or partial residual inhibition. This technique is based on the theory by Choy advocating that the induction of a sound wave with a 180 degree phase shift compared to the sound experienced by the patient could result in sound cancelling, likely by negation of the cortical perception of tinnitus.

The aim is to determine the efficacy of the Phase Out treatment in pure tone and narrow band noise tinnitus patients.


Recruitment information / eligibility

Status Completed
Enrollment 40
Est. completion date
Est. primary completion date March 2009
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- consult ENT department UZA with tinnitus

- pure tone tinnitus or narrow band noise tinnitus

- unilateral tinnitus, or bilateral tinnitus if both ears pure tone or both ears narrow band noise

- frequency tinnitus > 1kHz

- cochlear origin tinnitus

- tinnitus duration 3 months or longer

- age 18y or more

- patient being able to cooperate

- patiƫnt able to fill in VAS

- normal MRI pontine angle

Exclusion Criteria:

- depression: BDI > 21

- pulsatile tinnitus

- pregnancy

- epilepsy

Study Design

Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Device:
Phase Out treatment in pure tone tinnitus patients
Phase Out treatment: 30 min 3x/w during 6 weeks

Locations

Country Name City State
Belgium Antwerp university Hospital Edegem Antwerp

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Antwerp

Country where clinical trial is conducted

Belgium, 

Outcome

Type Measure Description Time frame Safety issue
Primary Visual Analogue Scale 3x/week No
Secondary Score on Tinnitus Questionnaire week 0, week 3, week 6 No
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