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Use of a Disk of Amniotic Membrane (Visio-AMTRIX) in Postoperative Care After PKR

Myopia Clinical Trial

Official title:
Study Comparing a Therapeutic Lens Used Alone to a Therapeutic Lens Used in Association With an Amniotic Membrane Treated by the AMTRIX Process in Postoperative Care After Photorefractive Keratectomy (PRK)

Clinical Trial Summary

The purpose of this open controlled multicenter trial is to assess the impact of use of an amniotic membrane on post PKR recovery.

Clinical Trial Description

Photorefractive keratectomy (PRK) and laser-assisted in situ keratomileusis (LASIK) are two of the most widely used techniques of laser vision correction. However, one of the major disadvantages of the PRK technique is the pain experienced during 1 to 3 days after intervention. Preliminary data on a limited number of patients tend to show a reduction of pain, tearing and discomfort in patients for whom a amniotic membrane was used under a therapeutic lens. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05247658
Study type Interventional
Source TBF Genie Tissulaire
Contact
Status Terminated
Phase Phase 3
Start date January 25, 2022
Completion date July 21, 2022
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