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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05268770
Other study ID # 202200148
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date March 2022
Est. completion date August 2022

Study information

Verified date February 2022
Source University Medical Center Groningen
Contact Lilian M Mennink, MD
Phone 0031503610522
Email l.m.mennink@umcg.nl
Is FDA regulated No
Health authority
Study type Observational [Patient Registry]

Clinical Trial Summary

Rationale: Tinnitus is the perception of sound without an external source. In the past decade, inflammation has been implicated in the pathophysiology of tinnitus. In animal models of tinnitus, the expression of proinflammatory cytokines Tumor Necrosis Factor-α (TNF-α) and interleukine-1β (IL-1β) was increased throughout the whole auditory tract. Only two studies evaluated cytokine concentrations in tinnitus patients. In these studies an increase of IL-6 and decrease of IL-10 have been objectified. However, studies did not include tinnitus patients based on the degree of hearing loss, despite that inflammation has also been implicated in hearing loss. On the other hand, studies about inflammation in hearing loss did not (always) exclude tinnitus. Thus, it remains unclear whether the upregulated cytokine concentrations the studies are specific for tinnitus, and whether potential effects remained unsignificant because the presence of hearing loss is a confounder. Therefore, the aim of this study is to evaluate the presence of inflammation in tinnitus patients with normal hearing. Objective: The main objective is to evaluate the presence of inflammation in blood samples of human subjects with tinnitus and normal hearing, compared to healthy controls. The secondary objective is to evaluate the relation between tinnitus severity and inflammatory marker concentrations. Study design: This is a cross-sectional study. Study population: Patients who have been referred to the tinnitus consultation at the outpatient clinic will be asked to participate in this study. For the control group, healthy volunteers will be recruited. Main study parameters/endpoints: The main study parameter is the disparity in blood cytokine levels between participants with and without tinnitus. Secondary study parameters are the relation between tinnitus severity and blood cytokine concentration, and the difference in complete blood count measures in participants with and without tinnitus.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 100
Est. completion date August 2022
Est. primary completion date August 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - To be eligible to participate in this study, a subject must meet all of the following criteria: - Adult, aged 18 years or older; - Hearing threshold: average of 1000kHz, 2000kHz & 4000kHz = 25 dB. - Anxiety score HADS = 7 - Depression score HADS = 7 - Participant has sufficient mastery of the Dutch language to fill out the questionnaires. - Psychosocially, mentally, and physically able to fully comply with this protocol. Exclusion Criteria: - Objective tinnitus. - Presence of neurological disease (apart from tinnitus) - Presence of inflammatory disease, or the use of anti-inflammatory medication. - Presence or history of a malignancy - Presence of a disease of the ear (e.g. chronic otitis media, otosclerosis, previous surgery etc). - Presence of an coagulation disorder - Presence of a serious psychiatric disorder. - Pregnancy

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
University Medical Center Groningen

Outcome

Type Measure Description Time frame Safety issue
Primary Tinnitus vs no tinnitus Difference in cytokine levels between participants with and without tinnitus September 2022
Secondary Tinnitus severity Relation between cytokine levels and tinnitus severity September 2022
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