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Multimodal Imaging in Central Serous Chorioretinopathy

Not Applicable
Terminated
Conditions
Central Serous Chorioretinopathy
Registration Number
NCT02889185
Lead Sponsor
Centre Hospitalier Universitaire de Besancon
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.

Detailed Description

Not available

Recruitment & Eligibility

Status
TERMINATED
Sex
All
Target Recruitment
3
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

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Primary Outcome Measures
NameTimeMethod
Workability of images of RTX1 IMAGIN EYE retinal cameraday 1

Two readings of the images captured with adaptative optics retinal camera and assessment of their workability in routine care.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

CHU Besançon

🇫🇷

Besançon, France

CHU Besançon
🇫🇷Besançon, France

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