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Clinical study of corneal stromal lens in corneal cross-linking surgery

Clinical study of corneal stromal lens in corneal cross-linking surgery

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300068037
Enrollment
Unknown
Registered
2023-02-03
Start date
2022-06-01
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

Keratoconus

Interventions

Lens thickening group:Thickened lens

Sponsors

West China Hospital of Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Progressive keratoconus (continuous corneal topography for at least 3 months); 2. Thickness of the thinnest point of cornea < 400um; 3. No other eye patients other than keratoconus, no eye-related systemic diseases; 4. No corneal contact lens wearing history within one month.

Exclusion criteria

Exclusion criteria: 1. Have ocular trauma, surgical history, glaucoma or other abnormal eye diseases; 2. Acute corneal infection or corneal edema; 3. Pregnancy and lactation.

Design outcomes

Primary

MeasureTime frame
the power of cornea;corneal endothelium;vision acuity;—

Countries

China

Contacts

Public ContactMA KE

West China Hospital, Sichuan University

280463919@qq.com+86 189 8060 6396

Outcome results

None listed

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