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The Effect of Wearing Orthokeratology on Objective Visual Quality

The Effect of Wearing Orthokeratology on Objective Visual Quality

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04929119
Enrollment
30
Registered
2021-06-18
Start date
2021-03-07
Completion date
2022-03-31
Last updated
2021-06-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Visual Quality

Keywords

Objective visual quality, Orthokeratology

Brief summary

The visual quality indexes of these patients before and after Orthokeratology treatment were compared: 4 mm higher strehl ratio (SR) , 4 mm higher order corneal aberrations (Hoa ) , Spherical Aberrations (SA) , Comas, Trefoil Aberrations (RMS) , corneal aspheric index (Q, e) , corneal surface regularity index (SRI) , corneal surface asymmetry index (Sai)

Detailed description

USING OPD-SCAN III instrument method: Drag The joystick to focus on the screen prompt, and the device automatically starts to measure the aberration when the yellow focus is shown; Simk will change from black to rose red when the aberration is measured to start measuring the corneal topography, prompting the patient to blink the tear film evenly and press the button on the joystick when the focus is completed.The following data were obtained and analyzed: 4 mm high order STREHL rate (SR) , 4 mm high order corneal aberration (Hoa ) , Spherical Aberration (SA) , Coma Aberration (Coma) , Trefoil Aberration (RMS) , corneal aspheric index (Q, e) , corneal surface regularity index (SRI) , corneal surface asymmetry index (Sai)

Interventions

None listed

Sponsors

XiaoYong Liu
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
8 Years to 25 Years
Healthy volunteers
No

Inclusion criteria

* The subject understands the purpose of this clinical trial and is willing, able and committed to return to the center for all clinical trial visits and to complete all research related procedures

Exclusion criteria

* 1\. Associated with corneal abnormalities, such as active Keratitis (corneal infection) , corneal dystrophy, Keratoconus, corneal Leukoplakia, corneal hypoesthesia, or previous corneal surgery, or a history of corneal trauma; * 2, there are other eye diseases, such as Dacryocystitis, dry eye disease, conjunctivitis, blepharitis, Uveitis, and other inflammation, Glaucoma, cataracts, fundus disease, eye tumors, ocular trauma, squint patients; * 3\. A history of allergy to contact lens or contact Lens Solution. * 4\. Test results indicate that subjects with contraindications or unsuitable for wearing Orthokeratology.

Design outcomes

Primary

MeasureTime frameDescription
4 mm high-order strehl ratio6 monthsObjective visual quality 1
4 mm high-order corneal aberrations (Hoa) in Microns6 monthsObjective visual quality 2
Spherical Aberrations (SA) in Microns6 monthsObjective visual quality 3
Coma Aberrations (COMA) in Microns6 monthsObjective visual quality 4
Trefoil Aberrations in Microns6 monthsObjective visual quality 5
corneal aspheric index(Q)6 monthsObjective visual quality 6
corneal aspheric index(e)6 monthsObjective visual quality 7
corneal surface regularity index (SRI)6 monthsObjective visual quality 8
corneal surface asymmetry index (Sai)6 monthsObjective visual quality 9

Countries

China

Contacts

Primary Contactxiaoyong Liu
jndxlxy@163.com86-13760638809

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 6, 2026