Determine the Incidence of Long QT Amongst a Large Cohort of Subjects Diagnosed With Unilateral or Bilateral Sensorineural Hearing Loss.

Pediatrix

Status: Completed

Conditions: Long QT Syndrome; Sensorineural Hearing Loss

Study type: Observational

Funder types: Other

Identifiers

NCT02082431

PDX-001-13

Details and patient eligibility

About

The purpose of this study is to determine the true incidence of long QT (LQT) amongst a large cohort of subjects diagnosed with unilateral (right/left) or bilateral sensorineural hearing loss.

Full description

The purpose of this study is to determine the true incidence of long QT (LQT) amongst a large cohort of subjects diagnosed with unilateral (right/left) or bilateral sensorineural hearing loss.

The goal of this study is to answer the following questions:

1. What is the incidence of an abnormal ECG (QTc > 450 msec) in neonates greater than a week of age with either unilateral or bilateral Sensorineural hearing loss?
2. What percentage of neonates greater than one week of age with either bilateral or unilateral sensorineural hearing loss and an abnormal ECG have an identifiable genetic mutation?
3. What is the incidence of an abnormal genetic mutation consistent with long QT regardless of the ECG in neonates with bilateral sensorineural hearing loss?

Enrollment: 600 estimated patients

Sex: All

Ages: 1 to 90 days old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• All newborns who demonstrate a refer in one or both ears on a routine newborn hearing screen
• Documentation of informed consent
• Inborn
• Ability to perform an ABR (auditory brainstem response screen technology) screening test
• No major anomalies
• Subjects' parents willing to provide follow-up data on their child

Exclusion criteria

• Newborns with a syndromic cause of hearing loss
• Parents unwilling to provide follow-up data
• Major congenital anomalies
• Major medical problem or conditions. (i.e., hypoxic ischemic encephalopathy (HIE), persistent pulmonary hypertension neonate (PPHN), meconium aspiration, etc.)
• Congenital cytomegalovirus (CMV)