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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00400413
Other study ID # 2865
Secondary ID
Status Completed
Phase N/A
First received November 15, 2006
Last updated August 29, 2011
Start date November 2003
Est. completion date August 2011

Study information

Verified date August 2011
Source University Hospital, Strasbourg, France
Contact n/a
Is FDA regulated No
Health authority France: Ministry of Health
Study type Interventional

Clinical Trial Summary

The aim of the research is to investigate phonological processing in deafness and to examine its influence on the neuroanatomy of reading.The basic hypothesis is that insofar as the ability to read is closely related to the ability to segment and represent speech units, the neuroanatomy of reading in deaf would be different from the one of hearing readers.


Recruitment information / eligibility

Status Completed
Enrollment 60
Est. completion date August 2011
Est. primary completion date
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years and older
Eligibility Inclusion criteria:

- adult

- full education

Exclusion criteria:

- reading impairment

- fMRI

Study Design

Allocation: Non-Randomized, Intervention Model: Single Group Assignment, Masking: Open Label


Related Conditions & MeSH terms


Intervention

Procedure:
fMRI


Locations

Country Name City State
France Clinique Neurologique - Hôpital Civil Strasbourg

Sponsors (4)

Lead Sponsor Collaborator
University Hospital, Strasbourg, France Conseil Régional d'Alsace, France: Centre National de la Recherche Scientifique, Institut National de la Santé Et de la Recherche Médicale, France

Country where clinical trial is conducted

France, 

See also
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Completed NCT00106743 - Natural History and Genetic Studies of Usher Syndrome
Terminated NCT03866850 - Degenerative Consequences of Congenital Deafness
Not yet recruiting NCT06370351 - A Phase I/II Clinical Trial With SENS-501 in Children Suffering From Severe to Profound Hearing Loss Due to Otoferlin (OTOF) Mutations Phase 1/Phase 2
Not yet recruiting NCT04350619 - NGS Assessment of Congenitally Deafned Children and Neonatal Deafness Screnning
Not yet recruiting NCT06365749 - Genetic Feature of Congenital Hearing Loss in Chinese Population