A clinical trial to study the comparison of hydrophilic intraocular lens and silicone lens in children undergoing cataract surgery
Not Applicable
Completed
- Registration Number
- CTRI/2010/091/000195
- Lead Sponsor
- Dr Jagat Ram
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 41
Inclusion Criteria
(a) Children, aged one month to eight years, with visually significant congenital or developmental cataract. (b) Partial or dense, visually significant cataract, involving 3 mm or more of the central visual axis
Exclusion Criteria
(a) Presence of an associated ocular disease such as microphthalmia, microcornea, glaucoma, uveitis, complicated cataract, posterior lenticonus, coloboma, subluxated lens, retinal lesions like retinal detachment, retinal holes etc. (b) Suspected pre existing posterior capsular defects like traumatic cataract (c) Systemic diseases (d) Children in whom the axial length of the eye < 17mm.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method visual axis opacification (VAO), PCO, membranectomy rates for significant VAOTimepoint: one year
- Secondary Outcome Measures
Name Time Method ILTimepoint: NI