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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00748475
Other study ID # TE0602-1
Secondary ID
Status Completed
Phase N/A
First received September 5, 2008
Last updated February 19, 2013
Start date September 2008

Study information

Verified date February 2013
Source University of Konstanz
Contact n/a
Is FDA regulated No
Health authority Germany: Ethics Commission
Study type Interventional

Clinical Trial Summary

The purpose of the study is to examine the effect of alpha-neurofeedback while subjects listen to a noise on tinnitus.


Recruitment information / eligibility

Status Completed
Enrollment 12
Est. completion date
Est. primary completion date May 2010
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria:

- Duration of Tinnitus >= 6 months and <= 20 years

- Subjective Tinnitus

Exclusion Criteria:

- History of neurological or more than mild psychiatric diseases

Study Design

Allocation: Non-Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Behavioral:
Neurofeedback


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
University of Konstanz

Outcome

Type Measure Description Time frame Safety issue
Primary Reduction of tinnitus distress using the Tinnitus Questionaire Before the first and after the last session. No
Primary Cortical Alpha Power Before the first and after the last session No
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