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Comparison of Ngenuity and Traditional Microscopy in Assessing Retinal Function Recovery Post-ICL Surgery

Comparison of Ngenuity and Traditional Microscopy in Assessing Retinal Function Recovery Post-ICL Surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500100116
Enrollment
Unknown
Registered
2025-04-02
Start date
2025-04-15
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

high myopia

Interventions

3D visualization system group:operation through 3D visualization system with coaxial illumination (3D-C) approach
standard operating microscope group:operation through standard operating microscope with standard illumination

Sponsors

Fuzhou Eye Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: 1. High myopia patients aged 18-40 years who have the intention to improve visual acuity through ICL surgery; 2. Stable refractive power (refractive change = 2.7 mm, open angle; 4. Corneal endothelial cell density >= 2000 cells/mm2.

Exclusion criteria

Exclusion criteria: Subjects with cataract, keratopathy, glaucoma, nystagmus, strabismus, lens subluxation, severe vitreoretinopathy, a history of trauma or surgery and other eye diseases were excluded.

Design outcomes

Primary

MeasureTime frame
b-wave of the maximal combined response;

Secondary

MeasureTime frame
a-wave of the maximal combined response;superficial retinal capillary plexus density;un-corrected visual acuity;best corrected visual acuity;

Countries

China

Contacts

Public ContactXiangyu Ye

Fuzhou Eye Hospital

lisary609@163.com+86 183 5010 6026

Outcome results

None listed

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