Pilot Study of Familial Nonsyndromal Mondini Dysplasia

Completed

Conditions studied: Mondini Dysplasia

In brief

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

Key facts

Study ID

NCT00004336

Run by

National Center for Research Resources (NCRR)

People needed

2

Starts

1995-10-01

Last updated by the study team

2005-06-24

Who can join

Age: any. Sex: any. Healthy volunteers: not accepted.

Where it is running

• University of Michigan Health Systems — Ann Arbor, Michigan, United States

Full record on ClinicalTrials.gov

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