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Clinical Study on Anterior Segment OCT- Guided Personalized Selection of ICL Models

Clinical Study on Anterior Segment OCT- Guided Personalized Selection of ICL Models

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600118438
Enrollment
Unknown
Registered
2026-02-05
Start date
2026-02-10
Completion date
Unknown
Last updated
2026-02-09

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

Conditions

Refractive error

Interventions

Group A:Conventional Clinical ICL Model Selection
Group B:Anterior Segment OCT-guided Personalized ICL Model Selection

Sponsors

Tianjin Medical University Eye Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Stable refractive status, defined as a change in spherical equivalent (SE) of =2.8 mm, as measured by ultrasound biomicroscopy (UBM) or anterior segment optical coherence tomography (AS-OCT), to ensure sufficient space for ICL implantation; 3. Sufficient corneal endothelial cell density (ECD) of >=2000 cells/mm² without significant endothelial dysfunction, indicating tolerance for the surgical procedure; 4. Normal ocular anatomy with no significant pathology such as corneal disorders, glaucoma, cataracts, retinal breaks or detachment, or uveitis. The same inclusion criteria were applied to the study subjects in both the retrospective and prospective phases of the research.

Exclusion criteria

Exclusion criteria: 1. Unstable refractive status, defined as a change in spherical equivalent (SE) of >0.50 diopters (D) over the past year or the presence of progressive refractive disorders such as uncontrolled pathological myopia; 2. Insufficient anterior chamber depth (ACD) of 21 mmHg or the presence of glaucoma risk factors such as a family history of glaucoma or narrow anterior chamber angles; 5. Retinal pathology, including retinal degenerative lesions, breaks, a previous history of retinal detachment, or severe vitreous opacity precluding adequate examination. The same exclusion criteria were applied to the study subjects in both the retrospective and prospective phases of the research.

Design outcomes

Primary

MeasureTime frame
ICL Vault Fitness Rate;

Secondary

MeasureTime frame
clinical safety;visual quality;

Countries

China

Contacts

Public ContactYang Ruibo

Tianjin Medical University Eye Hospital

yangruibo771@163.com+86 22 86428810

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 15, 2026