CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 324 enrolled / 324 target
Drug / intervention
Not specified
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00023036
NCT00023036N/ACompletedOn Track (1.1/mo)

Clinical and Molecular Analysis of Enlarged Vestibular Aqueducts

National Institute on Deafness and Other Communication Disorders (NIDCD)·observational·Posted Aug 22, 2001·Updated Jun 18, 2026

In Brief

An observational study for Sensorineural Hearing Loss and Cytomegalovirus Infection. Completed, enrolled 324 participants across 1 site.

Detailed Summary

This study will try to identify and understand the genetic factors that lead to an inner ear malformation called "enlarged vestibular aqueducts", that can be associated with hearing loss. Patients with sensorineural hearing loss with or without inner ear malformations and their parents and siblings may be eligible for this study. Participants and their immediate family members, may undergo some or all of the following tests and procedures: * Medical and family history, including questions about hearing, balance and other ear-related issues, and review of medical records. * Routine physical examination. * Blood draw or buccal swab (brushing inside the cheek to collect cells) - Tissue is collected for DNA analysis to look for changes in genes that may be related to hearing loss. * Hearing tests - The subject listens for tones emitted through a small earphone. * Balance test (VEMP) to see if balance functions of the inner ear are associated with the hearing loss Electrodes will be placed behind your ear and at the base of your neck. From a reclining position, you will be asked to raise your head while clicking sounds are played into your ears. - Ultrasound tests - An inner ear malformation called EVA (enlargement of the vestibular aqueduct) indicates that a genetic disorder called Pendred syndrome may be the cause. Because thyroid abnormalities are also associated with Pendred syndrome, an ultrasound examination of the thyroid gland may be done. * Computed tomography (CT) and magnetic resonance imaging (MRI) scans - These tests show the structure of the inner ear. For CT, the subject lies still for a short time while X-ray images are obtained. For MRI, the patient lies on a stretcher that is moved into a cylindrical machine with a strong magnetic field. The magnetic field and radio waves produce images of the inner ear. The radio waves cause loud thumping noises that can be muffled by the use of earplugs.

Study Details

Study Typeobservational
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

N/ACompletedFinished
200120022003200420052006200720082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedAug 22, 2001
Enrollment StartSep 4, 2001
TodayJul 2, 2026
Posted 24.9 years ago

Arms & Interventions

1other

Patients with known or suspected nonsyndromic SNHL associated with EVA

2other

Patients with nonsyndromic EVA

3other

unaffected siblings and parents of affected family members

4other

Other unaffected relatives; included if there is more than one sibship with affected family