Pilot Study of Familial Nonsyndromal Mondini Dysplasia

This study has been completed.
Sponsor:
Collaborator:
University of Michigan
Information provided by:
National Center for Research Resources (NCRR)
ClinicalTrials.gov Identifier:
NCT00004336
First received: October 18, 1999
Last updated: June 23, 2005
Last verified: April 2002

October 18, 1999
June 23, 2005
October 1995
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Complete list of historical versions of study NCT00004336 on ClinicalTrials.gov Archive Site
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Pilot Study of Familial Nonsyndromal Mondini Dysplasia
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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.

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.

Observational
Primary Purpose: Screening
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Mondini Dysplasia
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*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
2
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PROTOCOL ENTRY CRITERIA:

Parents of a study family with nonsyndromal Mondini dysplasia

Both
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No
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT00004336
199/11895, UMMC-1402
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National Center for Research Resources (NCRR)
University of Michigan
Study Chair: Andrew J. Griffith University of Michigan
National Center for Research Resources (NCRR)
April 2002

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP