Prospective Study Evaluating Dry Eye in Patients Operated on for Ametropia by LASIK Surgery and Treated With REPADROP

Hospices Civils de Lyon10 enrolled

Overview

LASIK is a refractive surgery technique widely used in France. Postoperatively, the classic treatment after LASIK consists of instilling drops to reduce dry eyes. REPADROP® is an innovative eye drops stimulating corneal innervation. To date no study has quantified the improvement in dry eye syndrome and thus the quality of life of patients using REPADROP®.

Study Type

OBSERVATIONAL

Enrollment

Conditions

Ametropia

Interventions

Describe the evolution of dry eye between 1 month and 3 months post-LASIKOTHER

Dry eye will be assessed through the OSDI (Ocular Surface Disease Index) questionnaire. The questionnaire will be dispensed during consultations by an orthoptist or an intern/junior doctor, at 1 month and at 3 months post-LASIK.

Eligibility

Sex: ALLMin age: 18 Years

Medical Language ↔ Plain English

Inclusion Criteria: Age over 18 * Planned bilateral LASIK surgery * Use of Repadrop as postoperative eye drops * Patient agreement to participate Exclusion Criteria: * History of corneal pathology * Diabetes * History of treatment with REPADROP® or CACICOL® or NGF® (other eye drops which are no longer available on the market to date but which would also improve corneal healing) * Ongoing treatment with topical cyclosporine * Presence of punctal plugs * Adults who are the subject of a legal protection measure (guardianship, curators) * Pregnant or breastfeeding women

Locations (1)

Hôpital Edouard Herriot

Lyon, Rhone, France

Outcomes

Primary Outcomes

Variation in OSDI (Ocular Surface Disease Index) score

Variation in OSDI (Ocular Surface Disease Index) score between 1 month and 3 months post-LASIK. The OSDI is assessed on a scale of 0 to 100, with higher scores representing greater disability.

Time frame: 3 Months

Data from ClinicalTrials.gov

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