Informations générales (source: ClinicalTrials.gov)
Bimodal and Coaxial High Resolution Ophtalmic Imaging (AOSLO-OCT)
Interventional
N/A
Centre Hospitalier National d'Ophtalmologie des Quinze-Vingts (Voir sur ClinicalTrials)
octobre 2019
octobre 2024
19 octobre 2024
The knowledge of the pathogenesis of retinal affections, a major cause of blindness, has
greatly benefited from recent advances in retinal imaging. However, optical aberrations
of the ocular media limit the resolution that can be achieved by current techniques.
The use of an adaptive optics system improves the resolution of ophthalmoscopes by
several orders of magnitude, allowing the visualization of many retinal microstructures:
photoreceptors, vessels, bundles of nerve fibers.
Recently, the development of the coupling of the two main imaging techniques, the
Adaptive Optics Ophthalmoscope with Optical Coherence Tomography, enables unparalleled
three-dimensional in vivo cell-scale imaging, while remaining comfortable for the
patients.
The purpose of this project is to evaluate the performance of this system for imaging
micrometric retinal structures.
Etablissements
Les établissements d'Île-de-France dont les données sont issues de ClinicalTrials.gov Origine et niveau de fiabilité des données | |||||
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CHNO DES QUINZE-VINGTS PARIS | Michel Paques, puph | Contact (sur clinicalTrials) |
Critères
Tous
Inclusion Criteria:
- People over 18
- Patient with a pathology affecting the eye or healthy volunteer
- Participant who signed the consent
- Beneficiaries of the health insurance
Exclusion Criteria
- Patients with a history of photosensitivity.
- Patients who have just received a photodynamic therapy treatment
- Patients taking drugs with photosensitivity as a side effect.
- Persons with pacemakers or other implanted electronic medical device
- Patients with viral conjunctivitis or any other infectious disease.
- Patients with skin lesions on the neck or forehead
- Patients at high risk of damage from optical radiation, such as aphakic patients, or
patients with decreased sensitivity to light due to fundus disease.
- Participant unable to be followed throughout the study
- Advanced cataract or severe opacities in the anterior segment of the eye.
- People over 18
- Patient with a pathology affecting the eye or healthy volunteer
- Participant who signed the consent
- Beneficiaries of the health insurance
Exclusion Criteria
- Patients with a history of photosensitivity.
- Patients who have just received a photodynamic therapy treatment
- Patients taking drugs with photosensitivity as a side effect.
- Persons with pacemakers or other implanted electronic medical device
- Patients with viral conjunctivitis or any other infectious disease.
- Patients with skin lesions on the neck or forehead
- Patients at high risk of damage from optical radiation, such as aphakic patients, or
patients with decreased sensitivity to light due to fundus disease.
- Participant unable to be followed throughout the study
- Advanced cataract or severe opacities in the anterior segment of the eye.