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Trial registered on ANZCTR
Registration number
ACTRN12619000291189
Ethics application status
Approved
Date submitted
19/02/2019
Date registered
26/02/2019
Date last updated
6/07/2021
Date data sharing statement initially provided
26/02/2019
Type of registration
Prospectively registered
Titles & IDs
Public title
Evaluation of the effects of primer sjögren's syndrome on the hearing and balance system
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Scientific title
INVESTIGATION OF PRIMARY SJOGREN SYNDROME EFFECTS ON HEARING AND VESTIBULAR SYSTEMS
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Secondary ID [1]
297139
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Nil known
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Primary sjögren's syndrome
311607
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Condition category
Condition code
Inflammatory and Immune System
310233
310233
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0
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Autoimmune diseases
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Ear
310234
310234
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0
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Other ear disorders
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Intervention/exposure
Study type
Observational
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Patient registry
False
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Target follow-up duration
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Target follow-up type
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Description of intervention(s) / exposure
This study is included that 35 volunteer patients(18-65 ages) diagnosed with primary Sjögren's syndrome by the Rheumatology clinic. Audiometry, Tympanometry, stapes reflex, VHIT (video head impulse test), cVEMP (cervical vestibular evoked myogenic potentials), and oVEMP (ocular vestibular evoked myogenic potentials) tests will be performed to patients following the ear-nose-throat examination. None of these tests are invasive tests. These tests keep on approximately 45 minutes.
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Intervention code [1]
313685
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Diagnosis / Prognosis
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Comparator / control treatment
35 healthy volunteers with similar age and gender with patients group will be included as a control group.
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Control group
Active
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Outcomes
Primary outcome [1]
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Detection of sensorineural hearing loss in the patients. The audiometry, tympanometry and stapes reflex tests will be used for this examination.
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Assessment method [1]
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Timepoint [1]
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After ear nose throat examination, the hearing test of the individuals will be performed by the audiologist.
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Secondary outcome [1]
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In order to detection of vestibular pathology, balance test (VEMP, VHIT) will be performed to individuals. Especially, it is important that the waves of VEMP are not obtained or detecting the increased latency time of waves or detection of asymmetric in semicircular canal's gain.
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Assessment method [1]
367024
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Timepoint [1]
367024
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After the hearing test, the balance test of the individuals will be performed by the audiologist.
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Eligibility
Key inclusion criteria
Individuals who primary Sjogren syndrome diagnosis
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Minimum age
18
Years
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Maximum age
65
Years
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Sex
Both males and females
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Can healthy volunteers participate?
Yes
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Key exclusion criteria
a. Conductive hearing loss
b. Patients with perforated tympanic membrane
c. Uncontrolled HT and/or diabetes mellitus
D. Patients with a previously diagnosed neuro-otological disease
e. Individuals who underwent head trauma
f. Individuals who performed cervical or eye-related surgery
g. Under 18 years and over 65 years
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Study design
Purpose
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Duration
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Selection
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Timing
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Statistical methods / analysis
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Recruitment
Recruitment status
Completed
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Date of first participant enrolment
Anticipated
4/03/2019
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Actual
4/03/2019
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Date of last participant enrolment
Anticipated
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Actual
24/11/2020
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Date of last data collection
Anticipated
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Actual
26/11/2020
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Sample size
Target
70
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Accrual to date
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Final
70
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Recruitment outside Australia
Country [1]
21287
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Turkey
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State/province [1]
21287
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Konya
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Funding & Sponsors
Funding source category [1]
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University
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Name [1]
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Selcuk University
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Address [1]
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Selcuk University Faculty of Medicine. Akademi Mah. Yeni Istanbul Cad. No:369 Post Code:42130
Selçuklu-Konya / TURKEY
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Country [1]
301699
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Turkey
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Primary sponsor type
University
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Name
Selcuk University
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Address
Selcuk University Faculty of Medicine. Akademi Mah. Yeni Istanbul Cad. No:369 Post Code:42130
Selçuklu-Konya / TURKEY
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Country
Turkey
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Secondary sponsor category [1]
301423
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None
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Name [1]
301423
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Address [1]
301423
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Country [1]
301423
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
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Selcuk University Faculty of Medicine
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Ethics committee address [1]
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Alaeddin Keykubat Campus, Akademi Mah. Yeni Istanbul Cad. No:369 Post Code:42130 Selçuklu-Konya / TURKEY
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Ethics committee country [1]
302418
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Turkey
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Date submitted for ethics approval [1]
302418
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30/05/2018
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Approval date [1]
302418
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27/06/2018
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Ethics approval number [1]
302418
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2018/252
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Summary
Brief summary
This study is included that 35 volunteer patients diagnosed with primary Sjogren's syndrome by the Rheumatology and 35 healthy volunteers with similar age and gender as a control group. Audiometry, Tympanometry, stapes reflex, VHIT (video head impulse test), cVEMP (cervical vestibular evoked myogenic potentials), and oVEMP (ocular vestibular evoked myogenic potentials) tests will be performed following the ear-nose-throat examination. None of these tests are invasive tests. As a result of this study, hearing and balance functions in patients with primary Sjogren diagnosis will be examined in comparison with the control group.
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Trial website
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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Dr Bülent Ulusoy
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Address
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Selcuk University faculty of medicine, Department of Otorhinolaryngology Head -Neck Surgery, Alaeddin Keykubat CAMPUS, Akademi Mah. Yeni Istanbul Cad. No:369 Post Code:42130
Selçuklu-Konya / TURKEY
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Country
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Turkey
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Phone
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+905065097893
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Fax
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Email
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[email protected]
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Contact person for public queries
Name
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Bülent Ulusoy
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Address
90179
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Selcuk University faculty of medicine, Department of Otorhinolaryngology Head -Neck Surgery, Alaeddin Keykubat CAMPUS, Akademi Mah. Yeni Istanbul Cad. No:369 Post Code:42130
Selçuklu-Konya / TURKEY
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Country
90179
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Turkey
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Phone
90179
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+905065097893
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Fax
90179
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Email
90179
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[email protected]
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Contact person for scientific queries
Name
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Bülent Ulusoy
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Address
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Selcuk University faculty of medicine, Department of Otorhinolaryngology Head -Neck Surgery, Alaeddin Keykubat CAMPUS, Akademi Mah. Yeni Istanbul Cad. No:369 Post Code:42130
Selçuklu-Konya / TURKEY
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Country
90180
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Turkey
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Phone
90180
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+905065097893
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Fax
90180
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Email
90180
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[email protected]
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Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
No
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No/undecided IPD sharing reason/comment
No - IPD will not be available
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What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
No additional documents have been identified.
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