Skip to content

Phase Out as a treatment for Tinnitus

Phase Out as a treatment for chronic untreatable tinnitus: a double blind crossover trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON23737
Enrollment
60
Registered
2007-03-12
Start date
2007-05-01
Completion date
Unknown
Last updated
2024-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

tinnitus, Phase Out, oorsuizen

Interventions

A subject will receive Phase Out treatment for thirty minutes three times a week for one week and placebo sound treatment on the same regime during another. One month interval is in between these two

Sponsors

Universitair Medisch Centrum Groningen
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Subjects > 18 years; 2. Unilateral or bilateral tinnitus; 3. Predominant tone tinnitus by history; 4. Tinnitus for minimum of 3 months;

Exclusion criteria

Exclusion criteria: 1. Acoustic neurinoma; 2. Aortic/ outflow tract stenosis; 3. Pulsatile tinnitus; 4. Pregnancy; 5. Inability to correct use of test equipment: unable to cooperate during audiologic examination; 6. Known tinnitus etiology, which would demand other treatment; 7. Hearing loss greater than 60 decibel compared with standardized normal hearing on standard frequencies of a tone audiogram (250; 500; 1000; 2000; 4000 en 8000 hertz).

Design outcomes

Primary

MeasureTime frame
The major aim of this study is disappearance (report mark) of the tinnitus lasting many hours (time).

Secondary

MeasureTime frame
Besides the mojor aims, different questionnaires will be used to determine for which kind of tinnitus patients, this treatment is most effective (THI, TRQ, VE, HADS, SF-36, Eysenck, type D personality, SSQ and TCSQ).

Contacts

Public ContactK.M. Heijneman

Universitair Medisch Centrum Groningen, afd. Keel-,Neus-, Oorheelkunde Postbox 30.001

k.m.heijneman@kno.umcg.nl+31503618053

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)