Otoacoustic Emissions in Different Blood Types
- Conditions
- Hearing Loss, Cochlear
- Interventions
- Diagnostic Test: Otoacoustic emissions (non-invasive)
- Registration Number
- NCT06326866
- Lead Sponsor
- Istanbul University - Cerrahpasa (IUC)
- Brief Summary
The objective of this study is to examine whether ABO and Rhesus (Rh) blood group systems have an association with distortion product otoacoustic emission (DPOAE) and transient otoacoustic emission (TEOAE) amplitudes with the hypothesis of blood groups may affect hearing thresholds.
- Detailed Description
Many factors have a significant impact on otoacoustic emission (OAE) measurement and quality of analysis. Race, age and gender are among the non-pathological factors. To date there is clear data to demonstrate the association of blood types with OAEs. The aim of our research is to investigate the relation of different blood groups (ABO) and Rh factors on transient evoked OAE and distortion product OAE amplitudes and inner ear potentials, differences between ears and to contribute to the limited literature on cochlear hearing loss susceptibility and blood groups with the hypothesis that blood groups may be associated with hearing thresholds.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 70
- not having hearing loss
- having a blood group card obtained from health institutions
- not meeting inclusion criteria
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Arm && Interventions
Group Intervention Description Individuals with B Rh (-) blood group Otoacoustic emissions (non-invasive) Individuals with normal hearing and whose blood group was previously determined as B Rh (-) will be included and and Transient evoked Otoacoustic Emissions (TOAE) and Distortion Product Otoacoustic Emissions (DPOAE) will be performed. Individuals with A Rh (+) blood group Otoacoustic emissions (non-invasive) Individuals with normal hearing and whose blood group was previously determined as A Rh (+) will be included and Transient evoked Otoacoustic Emissions (TOAE) and Distortion Product Otoacoustic Emissions (DPOAE) will be performed. Individuals with O Rh (+) blood group Otoacoustic emissions (non-invasive) Individuals with normal hearing and whose blood group was previously determined as O Rh (+) will be included and and Transient evoked Otoacoustic Emissions (TOAE) and Distortion Product Otoacoustic Emissions (DPOAE) will be performed. Individuals with O Rh (-) blood group Otoacoustic emissions (non-invasive) Individuals with normal hearing and whose blood group was previously determined as O Rh (-) will be included and and Transient evoked Otoacoustic Emissions (TOAE) and Distortion Product Otoacoustic Emissions (DPOAE) will be performed. Individuals with A Rh (-) blood group Otoacoustic emissions (non-invasive) Individuals with normal hearing and whose blood group was previously determined as A Rh (-) will be included and Transient evoked Otoacoustic Emissions (TOAE) and Distortion Product Otoacoustic Emissions (DPOAE) will be performed. Individuals with B Rh (+) blood group Otoacoustic emissions (non-invasive) Individuals with normal hearing and whose blood group was previously determined as B Rh (+) will be included and and Transient evoked Otoacoustic Emissions (TOAE) and Distortion Product Otoacoustic Emissions (DPOAE) will be performed. Individuals with AB Rh (+) blood group Otoacoustic emissions (non-invasive) Individuals with normal hearing and whose blood group was previously determined as AB Rh (+) will be included and and Transient evoked Otoacoustic Emissions (TOAE) and Distortion Product Otoacoustic Emissions (DPOAE) will be performed. Individuals with AB Rh (-) blood group Otoacoustic emissions (non-invasive) Individuals with normal hearing and whose blood group was previously determined as AB Rh (-) will be included and and Transient evoked Otoacoustic Emissions (TOAE) and Distortion Product Otoacoustic Emissions (DPOAE) will be performed.
- Primary Outcome Measures
Name Time Method Signal to noise ratios 1 month SNRs obtained for different frequencies in OAE In TEOAE, 1, 1.4, 2, 2.8, 4 kHz, in DPOAE 1, 1.4, 2, 2.8, 4, 6 kHz
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Eyyup KARA
🇹🇷İstanbul, Turkey