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3% Diquafosol Ophthalmic Solution Alter Ocular Surface parameter in Children Wearing Orthkeratology Lens

optometry,ophthalmology

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2200066859
Enrollment
Unknown
Registered
2022-12-20
Start date
2022-02-01
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

myopia,dry eye

Interventions

one:3% Diquafosol Ophthalmic Solution
two:3% Diquafosol Ophthalmic Solution+Wearing Orthkeratology

Sponsors

Changsha Aier Eye Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
8 Years to 18 Years

Inclusion criteria

Inclusion criteria: (1) Age > 8 years; (2) myopia from ?1.0D to ?5.5 DS, and with-the-rule astigmatism of up to ?1.75 DC or against-the-rule astigmatism of <-0.75 DC with keratometry from 41 to 46 D; (3) For the OrthoK wearers group, patients should have been able to master the wearing of OOK lenses and had worn them for 1 year; and (4) for the OrthoK Candidates group, all patients were the first time for orthkeratology and wore no glasses and contact lenses or used mainly frames before.(5) Participants with mild to moderate dry eye based on NIKTMH < 0.20mm or NIKBUT < 10s from Keratograph 5M examination adopted by the Dry Eye Workshop (DEWS) report were included

Exclusion criteria

Exclusion criteria: Participants who were had pathological changes of the lid margin or cornea, uvea, or retina, had other systemic diseases that may influence the ocular surface, and received other ocular treatment or surgeries.

Design outcomes

Primary

MeasureTime frame
Tear Film Break-up Time;Tear Meniscus Height;Dry Eye Questionnaire-5;blink pattern;meibomian gland score;

Countries

China

Contacts

Public ContactYang Zhikuan
287387544@qq.com13380071988

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026