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NCT01766596 Clinical Trial

Study the Signs of Ocular Degeneration in a Population Cohort (Dijon 3C Montrachet Cohort)

Glaucoma Clinical Trial

— 3C  

Official title:
Study the Signs of Ocular Degeneration in a Population Cohort (Dijon 3C Montrachet Cohort): Seek Correlations Between Signs of Neurological and Vascular Degeneration and Signs of Ocular Aging

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01766596
Other study ID # Creuzot-Garcher PHRC IR 2009
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date October 2009
Est. completion date November 4, 2019

Study information
Verified date April 2024
Source Centre Hospitalier Universitaire Dijon
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of the study proposed in Dijon is above all to focus on the possible relationship between age-related ocular pathologies (AMD and glaucoma) and et les degenerative neurological and cardiac pathologies. The principal objective is to seek in subjects who have undergone cerebral MRI and echocardiography, associations between the thickness of postganglionic fibers measured by Optical Coherence Tomography at the 7th year (n=1500) and signs of cerebral impairment (psycho-cognitive tests, circulation time, MRI signs). This association will be studied after taking into account the principal environmental (particularly dietary) and genetic risk factors.

Recruitment information / eligibility
Status Completed
Enrollment 1153
Est. completion date November 4, 2019
Est. primary completion date October 2013
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - Persons who have given their written consent - Persons who are taking part in the Dijon 3C study Exclusion Criteria: - Persons who are not registered with social security agency - Persons who are unable to sit upright during a consultation

Study Design

Related Conditions & MeSH terms

Intervention

Procedure:
• Optical Coherence Tomography

Locations
Country Name City State
France CHU Dijon Dijon

Sponsors (1)
Lead Sponsor Collaborator
Centre Hospitalier Universitaire Dijon

Country where clinical trial is conducted

France, 

Outcome
Type Measure Description Time frame Safety issue
Primary Measure the mean thickness of postganglionic fibers Measure the thickness of postganglionic fibers by Optical Coherence Tomography in the 4 quadrants of the peripapillary sclera. T=7 years of the 3C cohort
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