Study the Signs of Ocular Degeneration in a Population Cohort (Dijon 3C Montrachet Cohort)
3C
1 other identifier
interventional
1,153
1 country
1
Brief 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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Oct 2009
Longer than P75 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
October 1, 2009
CompletedFirst Submitted
Initial submission to the registry
January 10, 2013
CompletedFirst Posted
Study publicly available on registry
January 11, 2013
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 1, 2013
CompletedStudy Completion
Last participant's last visit for all outcomes
November 4, 2019
CompletedMay 1, 2024
April 1, 2024
4 years
January 10, 2013
April 30, 2024
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
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
Study Arms (1)
3C cohort
OTHERInterventions
Eligibility Criteria
You may qualify if:
- Persons who have given their written consent
- Persons who are taking part in the Dijon 3C study
You may not qualify if:
- Persons who are not registered with social security agency
- Persons who are unable to sit upright during a consultation
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
CHU Dijon
Dijon, 21000, France
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
January 10, 2013
First Posted
January 11, 2013
Study Start
October 1, 2009
Primary Completion
October 1, 2013
Study Completion
November 4, 2019
Last Updated
May 1, 2024
Record last verified: 2024-04