Skip to content

Research on the mechanism of aberration changes before and after wearing corneal reshaping lenses based on personalized eye models

Research on the mechanism of aberration changes before and after wearing corneal reshaping lenses based on personalized eye models

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2400080827
Enrollment
Unknown
Registered
2024-02-08
Start date
2024-03-01
Completion date
Unknown
Last updated
2024-02-11

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

Conditions

Myopia

Interventions

Case series :None

Sponsors

Tianjin Eye Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
8 Years to 13 Years

Inclusion criteria

Inclusion criteria: (1) Children aged 8-13 with myopia and astigmatism; (2) Diopter -1.00D~-4.00D; (3) Astigmatism = 1.50D; (4) Eye or systemic diseases that do not affect the wearing of corneal reshaping lenses

Exclusion criteria

Exclusion criteria: (1) One eye meets the inclusion criteria; (2) Those who suffer from systemic diseases resulting in immunocompromise, or those who have an effect on corneal reshaping (e.g., previous diabetes, Down's syndrome, rheumatoid arthritis, psychiatric disorders, etc., or those who have suffered from acute or chronic sinusitis within 1 year, etc.); (3) Those suffering from corneal anomalies, previous corneal surgeries or history of corneal trauma, or corneal hyperalgesia; (4) Those with the following symptoms in the eye: ? Active corneal infections of bacterial, fungal, or viral origin; ? Acute and chronic inflammation of the anterior segment of the eye other than the cornea, such as acute conjunctivitis and blepharitis; ? Any ocular disorder, injury, or structural abnormality that affects the cornea, conjunctiva, or eyelids, e.g., lachrymatorrhoea, glaucoma; ? Dry eye (Fluorescein Staining Tear Film Breakup Time (FBUT) = 5 s); ? Corneal staining = grade 2; ? Other pathological ocular congestion or redness. (5) Best-corrected distance visual acuity of less than 1.0 in either eye; (6) Corneal flat curvature (measured by corneal topographer) below 40.00D or above 46.00D; (7) Those with unstable refractive error; (8) Those with irregular corneal astigmatism; (9) Those with dominant strabismus; (10) Abnormal intraocular pressure (normal intraocular pressure ranges from 10 to 21 mmHg, and the difference in intraocular pressure between both eyes should be less than 5 mmHg); (11) Those with corneal endothelial cell density less than 2000 cells/mm2; (12) Those who have worn keratoplasty lenses within the previous 30 days; (13) Those with a history of allergy to contact lenses or contact lens care solutions; Individuals who are unable to undergo regular eye examinations (or whose relatives are unable to accompany minors on a regular basis).

Design outcomes

Primary

MeasureTime frame
Axis length;Corneal topography;Higher order aberration;Periretinal refraction;Open computer optometry;MRT multispectral retinal topography map;

Countries

China

Contacts

Public ContactXiaoqin Chen

Tianjin Eye Hospital Optometry Center

chenxq017@163.com+86 156 9224 5330

Outcome results

None listed

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