Modified Surgical Techniques for Pediatric Cataract Treatment
Cataract

About this trial
This is an interventional treatment trial for Cataract focused on measuring pediatric cataract, lens regeneration, endogenous lens epithelial stem cells, visual axis opacification, visual function
Eligibility Criteria
Inclusion Criteria:
- Age between 1 month and 24 months
- Uncomplicated congenital cataract (≥ 3 mm central dense opacity) in one or both eyes with an intact non-fibrotic capsular bag
- Informed consent signed by a parent or legal guardian
Exclusion Criteria:
- Intraocular pressure >21 mmHg
- Preterm birth (<28 weeks)
- Presence of other ocular diseases (keratitis, keratoleukoma, aniridia, glaucoma) or systemic disease (congenital heart disease, ischemic encephalopathy)
- History of ocular diseases (any congenital eye diseases, such as, congenital cataract, congenital glaucoma, congenital aniridia) in the family
- History of ocular trauma
- Microcornea
- Persistent hyperplastic primary vitreous
- Rubella
- Lowe syndrome
Sites / Locations
- Zhongshan Ophthalmic Center,Sun Yat-sen U
Arms of the Study
Arm 1
Arm 2
Experimental
Active Comparator
Modified technique for I/A group
Traditional technique for I/A group
In the modified cataract surgery procedure, the size of the capsulorhexis opening will be decreased to 1.0-1.5 mm in diameter. The capsulorhexis will be located in the peripheral area of the lens instead of the central area. A 0.9 mm phacoemulsification probe will be used to remove the cataractous lens. One drop of 0.5% or 1% atropine and an antibiotic/steroid ointment will be placed in the eye, which will then be patched.
• In traditional technique group, the cataractous lens will be removed through an anterior continuous curvilinear capsulorhexis (ACCC) that is about 5-6 mm in diameter.