Assessment of Corneal Biomechanical Properties Using Corvis ST Following LASIK, PRK, and CXL

NCT06818461 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 150

Last updated 2025-11-19

No results posted yet for this study

Summary

To evaluate corneal biomechanical changes using the Corvis ST in patients who have under-gone LASIK, PRK, and corneal cross-linking (CXL).

Conditions

  • Myopia
  • Keratoconus
  • Refractive Surgery

Interventions

OTHER

Corvis St Before and after lasik, PRK, CXL

corneal biomechanics measurment using corvis St

Sponsors & Collaborators

  • Beni-Suef University

    lead OTHER

Eligibility

Min Age
18 Years
Max Age
60 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2023-09-01
Primary Completion
2025-05-28
Completion
2025-10-31

Countries

  • Egypt

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06818461 on ClinicalTrials.gov