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Comparison of femtosecond laser-assisted astigmatic keratotomy and toric intraocular lens implantation for astigmatism correction in cataract surgery

Comparison of femtosecond laser-assisted astigmatic keratotomy and toric intraocular lens implantation for astigmatism correction in cataract surgery

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100051066
Enrollment
Unknown
Registered
2021-09-11
Start date
2021-10-01
Completion date
Unknown
Last updated
2022-05-16

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

Conditions

Cataract

Interventions

Toric group:toric intraocular lens implantation
FS-AK group:femtosecond laser-assisted astigmatic keratotomy

Sponsors

Eye Center of the Second Affiliated Hospital, School of Medicine, Zhejiang University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1. Patients over 18 years old who visited our hospital during the study period; 2. Corneal regular astigmatism is +0.75 D–+3.00 D; 3. Patients who plan to receive femtosecond laser-assisted cataract extraction combined with intraocular lens implantation in one eye; 4. It is expected that the best corrected visual acuity in one eye after surgery is better than 20/25; 5. Sign the informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients with irregular corneal astigmatism, corneal scar, keratoconus, pterygium and other diseases; 2. Patients with severe ocular inflammation, infection, high myopia, severe dry eye and other patients with poor control effect; 3. Previous pathological changes in the anterior segment (cornea, anterior chamber, sclera) or posterior segment (uveal, vitreous-retina), including retinal vascular occlusive disease, retinal detachment or peripheral retinal laser photocoagulation, age-related macular degeneration (ARMD), glaucoma, diabetic retinopathy, retinitis pigmentosa, and any optic nerve-related pathology; 4. Patients with a history of corneal and other eye surgery or trauma; 5. Patients with severe systemic diseases who are not suitable for surgery; 6. Patients with poor cooperation and mental illness; 7. Current or planned pregnancy or breastfeeding, or other conditions that cause changes in refractive status due to changes in hormone levels; 8. Those who are allergic to any perioperative medication in this study.

Design outcomes

Primary

MeasureTime frame
corneal astigmatism;

Secondary

MeasureTime frame
naked eye vision;Corrected vision;visual quality questionnaire;IOL rotation;

Countries

China

Contacts

Public ContactYao Ke

Eye Center of the Second Affiliated Hospital, School of Medicine, Zhejiang University

xlren@zju.edu.cn+86 571 87783907

Outcome results

None listed

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