Multimodal Imaging in Central Serous Chorioretinopathy

Centre Hospitalier Universitaire de Besancon1 site in 1 country3 target enrollmentApril 2016

ConditionsCentral Serous Chorioretinopathy

Overview

Phase: Not Applicable
Intervention: Not specified
Conditions: Central Serous Chorioretinopathy
Sponsor: Centre Hospitalier Universitaire de Besancon
Enrollment: 3
Locations: 1
Primary Endpoint: Workability of images of RTX1 IMAGIN EYE retinal camera
Status: Terminated
Last Updated: 6 years ago

Overview Investigators Eligibility Criteria Outcomes Sites Similar Trials

Overview

Brief Summary

This study aims to assess the contribution of the multimodal imaging, combining a routine examination using Optical Coherence Tomography (OCT) with an imaging procedure using adaptive optics retinal camera.

This is a feasibility study with a limited number of patients.

Registry

clinicaltrials.gov

Start Date

April 2016

End Date

December 4, 2018

Last Updated

6 years ago

Study Type

Interventional

Study Design

Single Group

Sex

All

Investigators

Sponsor

Centre Hospitalier Universitaire de Besancon

Responsible Party

Sponsor

Eligibility Criteria

Inclusion Criteria

•Signed informed consent form
•Beneficiary/affiliated to French social security/social healthcare
•Active ou chronic Central Serous Chorioretinopathy on at least one eye
•Absence of other known ophthalmological pathology or of any ophthalmological conditions revealed during the examination

Exclusion Criteria

•Legal incapacity or limited legal capacity
•Predictable poor adherence
•Subject without health insurance
•Pregnant or breatfeeding women
•Sujet étant dans la période d'exclusion d'une autre étude ou prévue par le "fichier national des volontaires"
•Presence of transparent medium opacity damaging images quality
•Previous photosensitivity
•Recent treatment with PhotoDynamic Therapy (PDT)
•Use of drugs inducing photosensitivity