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The objective of this research is to build a collection of non-invasive retinal imaging (OCT and OCTA) in order to investigate the incidence and impact of retinal damage in patients who have or have had COVID-19.
Full description
This monocentric study is aimed at 3 types of patients:
At the patient's inclusion, an ophthalmologic assessment will be performed including :
Fundus examination, optical coherence tomography (OCT) and optical coherence tomography angiography (OCTA) in all COVID-19 patients may detect retinal lesions. In addition, if a correlation is demonstrated between clinical and paraclinical parameters and between disease severity and retinal vascular damage in non-invasive imaging (OCT and OCTA), this would allow a better understanding of the pathophysiology of the disease, as well as factors that may influence disease severity and the mechanisms potentially responsible for the observed disorders.
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Inclusion criteria
Exclusion criteria
- Refusal of patient participation
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Central trial contact
Alexandra MIERE, MD; Camille JUNG, MD
Data sourced from clinicaltrials.gov
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