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Assessment of Corneal Biomechanical Properties Using Corvis ST and ECD Following LASIK, PRK, CXL, Veriflex IOL and Implantable Collamer Lens

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

Last updated 2026-07-02

No results posted yet for this study

Summary

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

Conditions

  • Myopia
  • Keratoconus
  • Refractive Surgery

Interventions

OTHER

Corvis St Before and after lasik, PRK, CXL, Veriflex IOL and ICL

corneal biomechanics measurment using corvis St and corneal endothelial cell counts

Sponsors & Collaborators

  • Beni-Suef University

    lead OTHER

Eligibility

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

Timeline & Regulatory

Start
2025-01-01
Primary Completion
2025-06-28
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