Pilot Study of Familial Nonsyndromal Mondini Dysplasia

NCT ID: NCT00004336

Last Updated: 2005-06-24

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

2 participants

Study Classification

OBSERVATIONAL

Study Start Date

1995-10-31

Brief Summary

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OBJECTIVES:

I. Determine the mode of inheritance of nonsyndromal Mondini inner ear dysplasia, an inner ear malformation causing deafness, vestibular dysfunction, and recurrent meningitis.

Detailed Description

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PROTOCOL OUTLINE:

The parents of 1 family with known Mondini dysplasia are screened for the disorder using temporal bone computerized tomography without contrast. This information is used to determine the mode of inheritance.

Conditions

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Mondini Dysplasia

Eligibility Criteria

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Inclusion Criteria

PROTOCOL ENTRY CRITERIA:

Parents of a study family with nonsyndromal Mondini dysplasia
Minimum Eligible Age

0 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University of Michigan

OTHER

Sponsor Role collaborator

National Center for Research Resources (NCRR)

NIH

Sponsor Role lead

Principal Investigators

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Andrew J. Griffith

Role: STUDY_CHAIR

University of Michigan

Locations

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University of Michigan Health Systems

Ann Arbor, Michigan, United States

Site Status

Countries

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United States

Other Identifiers

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UMMC-1402

Identifier Type: -

Identifier Source: secondary_id

199/11895

Identifier Type: -

Identifier Source: org_study_id