Assessment of Corneal Biomechanics With the Corvis ST in Different Age of Myopia With Orthokeratology
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Myopia
- Sponsor
- Tianjin Eye Hospital
- Enrollment
- 134
- Locations
- 1
- Primary Endpoint
- The change of dynamic corneal response (DCR)
- Status
- Completed
- Last Updated
- 3 years ago
Overview
Brief Summary
The present research focused on the effect of the age for the corneal biomechanics of low and moderate myopia patients after wearing orthokeratology (OK lens). According to age, the included cases were divided into 3 groups. Through the analysis of corneal biomechanical parameters, further learn the influence of OK lens on the patient cornea. It would help ophthalmologist and optometrist find out the potential issue and reach a better control result.
Detailed Description
The present research focused on the effect of the age for the corneal biomechanics of low and moderate myopia patients after wearing orthokeratology (OK lens). According to age, the included cases were divided into 3 groups: Ⅰ (8-12 years old), Ⅱ (13-16 years old), Ⅲ (over 16 years old). The OK lenses used in the present study are of the same design (Euclid Systems Orthokeratology; Euclid System, Herndon, VA, USA). The base line (Day 0) and different follow-up time point (Day 1, Week 1, Week 2, Month 1, Month 3, and Month 6) of dynamic corneal response (DCR) (including 19 items) of the patients derived by Corvis ST were collected. The difference between before and after wearing OK Lens and the changes of parameters among the three groups were both analyzed. And the correlation between axis length (AL) and the 19 parameters also was analyzed. Through the analysis of corneal biomechanical parameters, further learn the influence of OK lens on the patient cornea. It would help ophthalmologist and optometrist find out the potential issue and reach a better control result.
Investigators
Eligibility Criteria
Inclusion Criteria
- •age from 8 to 40 years old
- •spherical equivalent(SE) was range from -1.00D to -5.00D
- •conform to the standard of wearing orthokeratology lens
Exclusion Criteria
- •ocular diseases and systemic diseases
- •visual acuity was less than 20/20
- •unable to follow visitors on time
Outcomes
Primary Outcomes
The change of dynamic corneal response (DCR)
Time Frame: The change of baseline and 1 day, 1 week, 2 weeks, 1 month, 3 months, and 6 months
The axial length was measured by Corvis ST
Secondary Outcomes
- The change of axial length(The change of baseline and 6 months)