Mode of Delivery on Newborn Hearing Test

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

1000 participants

Study Classification

OBSERVATIONAL

Study Start Date

2017-01-01

Study Completion Date

2019-06-01

Brief Summary

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Neonatal hearing screening may fail due to some perinatal and neonatal factors. It is well known that false positivity increases cost and maternal anxiety and anxiety in the neonatal hearing screening. The effect of the type of delivery to hearing screening is not yet clear. The first automated mode of delivery of babies born in Turkey auditory brainstem response (SAD's), the authors aimed to evaluate the effects of the test results and false positive rate.

newborns were evaluated with brainstem response test. The AABR test was performed before patients were discharged. Perinatal and neonatal variables and AABR test results were recorded retrospectively.

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Detailed Description

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Conditions

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Hearing Loss, Neonatal

Study Design

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Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Eligibility Criteria

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Inclusion Criteria

* records of birth process and
* pregnancy test results of newborns.

Exclusion Criteria

* newborn;
* She was in a neonatal intensive care,
* congenital / chromosomal anomaly,
* undergoing congenital cmv infection,
* facial / ear deformity,
* families with hearing problems,
* those with hyperbiliromyemia,
* \<12 hours after delivery,
* maternal infection,
* dm,
* recurrent abortion,
* smoking,
* plesanta previa,

Minimum Eligible Age

18 Years

Maximum Eligible Age

40 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No