FindTrial
Sign In

Clinical Study of LenSx Femtosecond Laser-assisted Corneal Limbal Relaxing for Low and Moderate Astigmatism in posterior chamber intraocular lens implantation

Clinical Study of LenSx Femtosecond Laser-assisted Corneal Limbal Relaxing for Low and Moderate Astigmatism in posterior chamber intraocular lens implantation

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900023743
Enrollment
Unknown
Registered
2019-06-10
Start date
2019-07-01
Completion date
Unknown
Last updated
2019-06-17

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

Conditions

High myopia with low to moderate astigmatism

Interventions

control group 1:Implantation of ICL
control group 2:Implantation of TICL
experimental group:Implantation of ICL and Femtosecond Laser-assisted LRI

Sponsors

Chongqing Aier-Mega Eye Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.meet a criterion with the basic conditions of ICL; 2.The astigmatism ranges from - 0.75D to - 1.50D; 3.After the astigmatism was removed, the visual acuity chart dropped by a row; 4.Patients do not intend to consider Toric ICL 5.Be rational of advantages and disadvantages of surgery.

Exclusion criteria

Exclusion criteria: 1.Other ocular diseases affecting Visual acuity; 2.Keratoconus or suspected keratoconus.

Design outcomes

Primary

MeasureTime frame
Visual acuity;Comprehensive optometry;Surgical induced astigmatism;Target induced astigmatism;Correction index;High order aberration;modulation transfer function;—

Countries

China

Contacts

Public ContactPeng Yanli

Aier School of Ophthalmology, Central South University

243684965@qq.com+86 13618267642

Outcome results

None listed

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