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Clinical Trial Summary

The purpose of this open, monocenter pilot trial is to evaluate the tolerance of the SclerFIX product, an allograft of umbilical cord lining membrane, in the reinforcement of ocular implants in patients who underwent enucleation due to an eye malignant tumor resection.


Clinical Trial Description

As scleral graft is forbidden in France, it cannot be used for support of enucleation implants. This study investigational product, SclerFIX, was developed to substitute scleral grafts in those cases. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05236049
Study type Interventional
Source TBF Genie Tissulaire
Contact
Status Completed
Phase Phase 1
Start date July 1, 2019
Completion date April 27, 2022

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