Informations générales (source: ClinicalTrials.gov)
High Resolution and High Speed Multimodal Ophthalmic Imaging (IMA-MODE)
Interventional
N/A
Centre Hospitalier National d'Ophtalmologie des Quinze-Vingts (Voir sur ClinicalTrials)
juillet 2019
juillet 2027
16 octobre 2024
Knowledge of the pathogenesis of ocular conditions, a leading cause of blindness, has
benefited greatly from recent advances in ophthalmic imaging. However, current clinical
imaging systems are limited in resolution, speed, or access to certain structures of the
eye.
The use of a high-resolution imaging system improves the resolution of ophthalmoscopes by
several orders of magnitude, allowing the visualization of many microstructures of the
eye: photoreceptors, vessels, nerve bundles in the retina, cells and nerves in the
cornea.
The use of a high-speed acquisition imaging system makes it possible to detect functional
measurements such as the speed of blood flow. The combination of data from multiple
imaging systems to obtain multimodal information is of great importance for improving the
understanding of structural changes in the eye during a disease.
The purpose of this project is to observe structures that are not detectable with
routinely used systems.
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, PU-PH | 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
- People over 18
- Patient with a pathology affecting the eye or healthy volunteer
- Participant who signed the consent
- Beneficiaries of the health insurance
- 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.
- Pregnant or lactating women
- Participant unable to be followed throughout the study
- Vulnerable people
- Subjects with predisposition to closure of the iridocorneal angle