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NCT02891694: MERCURE

Metalloproteinases and Recurrent Corneal Erosion Syndrome

Completed Last updated 10 December 2020
What this trial tests

trial testing in vitro immuno-histo-chemical analysis of corneal epithelium in Recurrent Corneal Erosion Syndrome in 19 participants. Completed in 26 November 2020.

Timeline
2 December 2016
Primary endpoint
26 June 2020
26 November 2020

Quick facts

Lead sponsorFondation Ophtalmologique Adolphe de Rothschild
StatusCompleted
Study typeOBSERVATIONAL
Enrollment19
Start date2 December 2016
Primary completion26 June 2020
Estimated completion26 November 2020
Sites1 location across France

Drugs / interventions tested

Conditions studied

Sponsor

Fondation Ophtalmologique Adolphe de Rothschild — full company profile →

Who can join

18 and older, any sex, with Recurrent Corneal Erosion Syndrome. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Recurrent corneal erosion (RCE) syndrome can be observed either in the context of a dystrophy of the basement membrane or following corneal trauma. This syndrome is characterized by recurrent episodes of ocular pain more or less associated with localized separations between the outer epithelium and the epithelial basal lamina (basement membrane) because of anchorage abnormalities between these two corneal layers. This could be the result of an increased expression of metalloproteinases cleaving the hemidesmosomes which anchor epithelium to the basement membrane. The investigators hypothesis is that episodes of RCEs are favored by a hyper- expression of matricial metalloprotease 9 (MMP-9) induced by EMMPRIN and Galectin-3. The identification of such induction could lead to development of therapeutics inhibiting EMMPRIN and Galectin- 3 in the RCE syndrome.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. CD147/Basigin: From Integrative Molecular Hub to Translational Therapeutic Target.
    Yang XM, Bian H, Chen ZN. · · 2026 · cited 1× · PMID 41454696 · DOI 10.1002/advs.202518884

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Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing