CD160 Expression in Retinal Vessels is Associated With Retinal Neovascular Diseases
NCT ID: NCT03940664
Last Updated: 2019-05-07
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
75 participants
OBSERVATIONAL
2008-01-31
2017-07-31
Brief Summary
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* to analyze CD160 expression in both normal and pathological eyes from human adults
* to evaluate association between CD160 presence on endothelial cells from blood vessels and retinal vascular disease
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Detailed Description
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CD160 appeared in several experimental studies as a marker of activated endothelial cells, suggesting it could represent a promising target for novel anti-angiogenic.
Conditions
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Study Design
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CASE_CONTROL
RETROSPECTIVE
Study Groups
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neovascular group
patients with diabetic retinopathy, retinal vein occlusion complicated with iris rubeosis or neovascular glaucoma, ocular ischaemic syndrome, neovascular glaucoma secondary to any ocular event or iris rubeosis secondary to retinal detachment
immunohistochemistry on Formalin fixed and paraffin embedded blocks
non-neovascular group
patients without neovascular diseases or complications but who underwent events leading to eye surgery such as trauma, endophthalmitis, cellulitis, anterior perforation, corneal abscess or retinal detachment.
immunohistochemistry on Formalin fixed and paraffin embedded blocks
Interventions
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immunohistochemistry on Formalin fixed and paraffin embedded blocks
Eligibility Criteria
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Inclusion Criteria
* Patients who agree to participate to the study
* Major patient
Exclusion Criteria
* Minor patient
18 Years
ALL
No
Sponsors
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CHU de Reims
OTHER
Responsible Party
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Locations
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Chu Reims
France, Reims, France
Countries
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References
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Henry A, Boulagnon-Rombi C, Menguy T, Giustiniani J, Garbar C, Mascaux C, Labrousse M, Milas C, Barbe C, Bensussan A, Durlach V, Arndt C. CD160 Expression in Retinal Vessels Is Associated With Retinal Neovascular Diseases. Invest Ophthalmol Vis Sci. 2018 Jun 1;59(7):2679-2686. doi: 10.1167/iovs.18-24021.
Other Identifiers
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2018Ao001
Identifier Type: -
Identifier Source: org_study_id
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