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ENROLLING BY INVITATION
NCT07133737

5 Year Follow up of SMILE® Procedure for the Correction of Hyperopia

Sponsor: Gemini Eye Clinic

View on ClinicalTrials.gov

Summary

The planned study will investigate and evaluate refractive stability, predictability, and safety in patients who underwent SMILE® pro surgery for hyperopia with or without astigmatism at least five years ago. This study aims to gain long-term insights into the predictability, safety, stability and side effects of the SMILE® pro procedure. It will evaluate the refractive outcome so the findings can optimize treatment nomograms and selection criteria while providing evidence of the long-term stability and predictability of the procedure. Approximately 100 patients in the Czech Republic and Germany will participate in this study. The study was reviewed and approved by an independent research ethics committee.The study will consist of a single visit, where standard, non-invasive and painless examinations will be performed. The course of this visit will correspond to the patient's last visit five years ago as part of the clinical trial

Official title: Follow-up Study of at Least 5 Years After a SMILE® Pro Procedure for the Correction of Hyperopia Investigating Long-term Visual Outcomes and Potential Side Effects

Key Details

Gender

All

Age Range

Any - Any

Study Type

OBSERVATIONAL

Enrollment

100

Start Date

2025-01-01

Completion Date

2025-12-31

Last Updated

2025-08-21

Healthy Volunteers

No

Conditions

Locations (2)

Gemini Eye Clinic

Zlín, Czechia

Universitätsklinikum Marburg - Klinik für Augenheilkunde

Marburg, Germany