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

NCT ID: NCT06818461

Last Updated: 2025-11-19

Basic Information

• Recruitment Status: COMPLETED
• Total Enrollment: 150 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2023-09-01
• Study Completion Date: 2025-10-31

Brief Summary

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

Detailed Description

This observational study aims to evaluate corneal biomechanical changes in patients who have undergone LASIK, PRK, and corneal cross-linking (CXL) using the Corvis ST (Oculus). A total of 90 patients will be recruited from the ClearVision Laser Center database between January 2025 and December 2025. Participants will undergo non-contact biomechanical assessments at multiple postoperative time points to track corneal stability and elasticity over time.

Data Collection & Measurements Patient demographics, clinical history, and baseline preoperative data, including corneal thickness (pachymetry) and refractive status, will be collected. The Corvis ST will be used to measure key biomechanical parameters, such as Corneal Deformation Amplitude (CDA), Applanation Times (A1T & A2T), Radius of Curvature at Highest Concavity (RHC), Stiffness Parameter (SP-A1), Integrated Radius (IR), and the Corvis Biomechanical Index (CBI).

Measurement Protocol

All measurements will be conducted in a controlled environment with stable room temperature and humidity. Patients will be properly aligned, and three consecutive measurements per eye will be taken to ensure repeatability. Data will be recorded at specific intervals:

LASIK & PRK: 1 month, 3 months, 6 months, and 12 months CXL: 1 month, 3 months, 6 months, 12 months, and 24 months Potential Benefits & Risks The study aims to provide valuable insights into corneal biomechanical stability post-surgery, improving postoperative management and long-term visual outcomes. Risks are minimal, with only transient discomfort associated with the non-invasive Corvis ST measurements.

This study will contribute to a better understanding of corneal biomechanics in refractive and therapeutic procedures, potentially guiding future surgical decisions and patient care strategies.

Conditions

Myopia; Keratoconus; Refractive Surgery

Study Design

• Observational Model Type: CASE_CONTROL
• Study Time Perspective: PROSPECTIVE

Study Groups

Lasik

a non-contact air puff tonometer combined with Scheimpflug imaging to assess the cornea's deformation response. Measurements will be taken at multiple postoperative time points to track biomechanical changes. Key parameters such as Deformation Amplitude (DA), Stiffness Parameter (SP-A1), Applanation Times (A1 \& A2), Peak Distance (PD), and Biomechanically Corrected IOP (bIOP) will be recorded.

Corvis St Before and after lasik, PRK, CXL

Intervention Type: OTHER

corneal biomechanics measurment using corvis St

PRK

a non-contact air puff tonometer combined with Scheimpflug imaging to assess the cornea's deformation response. Measurements will be taken at multiple postoperative time points to track biomechanical changes. Key parameters such as Deformation Amplitude (DA), Stiffness Parameter (SP-A1), Applanation Times (A1 \& A2), Peak Distance (PD), and Biomechanically Corrected IOP (bIOP) will be recorded.

Corvis St Before and after lasik, PRK, CXL

Intervention Type: OTHER

corneal biomechanics measurment using corvis St

CXL

a non-contact air puff tonometer combined with Scheimpflug imaging to assess the cornea's deformation response. Measurements will be taken at multiple postoperative time points to track biomechanical changes. Key parameters such as Deformation Amplitude (DA), Stiffness Parameter (SP-A1), Applanation Times (A1 \& A2), Peak Distance (PD), and Biomechanically Corrected IOP (bIOP) will be recorded.

Corvis St Before and after lasik, PRK, CXL

Intervention Type: OTHER

corneal biomechanics measurment using corvis St

Interventions

Corvis St Before and after lasik, PRK, CXL

corneal biomechanics measurment using corvis St

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

• 1. Adults aged 18-60 years. 2. Patients who have undergone LASIK, PRK, or CXL at least 1 month prior to measure-ment.

3. Stable refraction for at least 3 months post-procedure. 4. No evidence of active ocular disease or infection.

Exclusion Criteria

• 1. History of other ocular surgeries (excluding LASIK, PRK, or CXL). 2. Presence of keratoconus or other corneal ectatic disorders not treated with CXL.

3. Systemic or ocular conditions affecting corneal biomechanical properties (e.g., dia-betes, connective tissue disorders).

4. Current or recent use of medications influencing corneal biomechanics.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 60 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Beni-Suef University

OTHER

Sponsor Role: lead

Responsible Party

Mohamed Yasser Sayed Saif

Professour of Ophthalmology

Responsibility Role: PRINCIPAL_INVESTIGATOR

Locations

Clearvision

Mohandessin, Giza Governorate, Egypt

Countries

Egypt

References

Luce DA. Determining in vivo biomechanical properties of the cornea with an ocular response analyzer. J Cataract Refract Surg. 2005 Jan;31(1):156-62. doi: 10.1016/j.jcrs.2004.10.044.

Reference Type: BACKGROUND

PMID: 15721708 (View on PubMed)

Other Identifiers

FMBSUREC/05012025/ Saif

Identifier Type: -

Identifier Source: org_study_id