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N/A Completed N=59 Treatment

Corneal Biomechanics and Corneal Reshaping Therapy

Source: ClinicalTrials.gov NCT02719535 ↗
Enrolled (actual)
59
Serious AEs
0.0%
Results posted
Apr 2020
Primary outcomePrimary: Change of Corneal Stiffness From Baseline at 6 Months — 0.061 N/mm

Summary

The aim of the proposed study is to investigate the predictive value of corneal biomechanical properties in corneal reshaping therapy and the role of these parameters in determining the amount of myopia reduction.

Outcome Measures

OutcomeResultp-value
PRIMARY
Change of Corneal Stiffness From Baseline at 6 Months
0.061
SECONDARY
Change of Tangent Modulus From Baseline at 6 Months
0.536

Eligibility Criteria

Inclusion Criteria

  • Myopia between -4D to -5D, with-the-rule astigmatism not more than 1.5D, spherical equivalent between -4D to -5.75D, difference between two eyes within 1D, best corrected spectacle visual acuity 0.10 logMAR in each eye

Exclusion Criteria

  • previous corneal reshaping therapy, long-term contact lens wear, ocular disease
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02719535). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.

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