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

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ClinicalTrials.gov Identifier: NCT01766596
Recruitment Status : Active, not recruiting
First Posted : January 11, 2013
Last Update Posted : September 1, 2016
Sponsor:
Information provided by (Responsible Party):
Centre Hospitalier Universitaire Dijon

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.


Condition or disease Intervention/treatment Phase
AMD Glaucoma Procedure: Optical Coherence Tomography Not Applicable

Study Type : Interventional  (Clinical Trial)
Estimated Enrollment : 3000 participants
Intervention Model: Single Group Assignment
Masking: None (Open Label)
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
Study Start Date : October 2009
Actual Primary Completion Date : October 2013

Resource links provided by the National Library of Medicine


Arm Intervention/treatment
3C cohort Procedure: Optical Coherence Tomography



Primary Outcome Measures :
  1. Measure the mean thickness of postganglionic fibers [ Time Frame: T=7 years of the 3C cohort ]
    Measure the thickness of postganglionic fibers by Optical Coherence Tomography in the 4 quadrants of the peripapillary sclera.



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Ages Eligible for Study:   Child, Adult, Older Adult
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

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

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01766596


Locations
France
CHU Dijon
Dijon, France, 21000
Sponsors and Collaborators
Centre Hospitalier Universitaire Dijon

Responsible Party: Centre Hospitalier Universitaire Dijon
ClinicalTrials.gov Identifier: NCT01766596     History of Changes
Other Study ID Numbers: Creuzot-Garcher PHRC IR 2009
First Posted: January 11, 2013    Key Record Dates
Last Update Posted: September 1, 2016
Last Verified: August 2016

Keywords provided by Centre Hospitalier Universitaire Dijon:
Ophthalmology
Age-related ocular pathologies