N/A N=59 Treatment

Corneal Biomechanics and Corneal Reshaping Therapy

Myopia

Bottom Line

View on ClinicalTrials.gov: NCT02719535 ↗

Enrolled (actual)

Serious AEs

0.0%

Results posted

Apr 2020

Primary outcome: Primary: Change of Corneal Stiffness From Baseline at 6 Months — 0.061 N/mm

Study Design & Population

Study type: Interventional
Phase: N/A
Interventions: Corneal reshaping therapy (Other)
Age: Adult · 18+ yrs
Sex: All
Sponsor: The Hong Kong Polytechnic University
Primary completion: Sep 2018

Outcome Measures

Outcome	Result	p-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	—

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.

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.