Femtosecond Laser Arcuate Keratotomy Versus Toric Intraocular Lens Implantation in Cataract Surgery
- Conditions
- CataractAstigmatism
- Registration Number
- NCT06215807
- Lead Sponsor
- Second Affiliated Hospital, School of Medicine, Zhejiang University
- Brief Summary
In modern cataract surgery, residual astigmatism continues to be one of the major factors influencing patients' visual quality and satisfaction. The goal of this study is to compare the clinical outcomes of femtosecond laser arcuate keratotomy in one eye and Toric intraocular lens implantation in the contralateral eye for astigmatism correction in patients undergoing femtosecond laser-assisted cataract surgery. The study is a prospective randomized comparative study. Patients with binocular regular corneal astigmatism ranging from 0.75 to 3.00 D will be recruited. The patient will randomly receive femtosecond laser arcuate keratotomy in one eye and receive Toric intraocular lens implantation in the contralateral eye. Long term evaluation will be performed to compare the visual acuity, subjective manifest refraction, and corneal topography between groups.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 200
- cataract patients
- patients with binocular regular corneal astigmatism ranging from 0.75 to 3.00 D
- patients who plan to receive femtosecond laser-assisted cataract surgery
- patients with ocular surface abnormalities such as irregular corneal astigmatism, corneal scarring, keratoconus, and pterygium)
- patients with history of ocular trauma or surgery
- patients with coexisting ocular disorders such as glaucoma, retinal vascular occlusive disease, retinal detachment, diabetic retinopathy, and any optic nerve-related pathologies
- patients with concurrent severe systemic diseases
- patients who lack of cooperation
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
Name Time Method Refractive astigmatism 1 day, 1 week, 1 month, 3 months and 1year postoperatively subjective manifest refraction and residual astigmatism
- Secondary Outcome Measures
Name Time Method Visual acuity 1 day, 1 week, 1 month, 3 months and 1year postoperatively uncorrected distance visual acuity and corrected distance visual acuity
Trial Locations
- Locations (1)
Eye Center of the Second Affiliated Hospital of Zhejiang University
🇨🇳Hangzhou, Zhejiang, China
Eye Center of the Second Affiliated Hospital of Zhejiang University🇨🇳Hangzhou, Zhejiang, ChinaYueyang ZhongPrincipal Investigator