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A clinical trial to study the comparison of hydrophilic intraocular lens and silicone lens in children undergoing cataract surgery

Comparitive study of visual performance following implantation of square edge hydrophobic acrylic and silicone intraocular lenses in pediatric cataract

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2010/091/000195
Enrollment
41
Registered
2010-03-15
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

None listed

Interventions

Intervention1: AcrySof SA60AT&reg
intra ocular lens (IOL): Control Intervention1: silicone, Tecnis Z9000&reg
IOL:

Sponsors

Dr Jagat Ram
Lead Sponsor
Sushma bhusal,jaspreet sukhija,surinder pandav,sushmita Kkaushik
Collaborator

Eligibility

Inclusion criteria

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

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.

Design outcomes

Primary

MeasureTime frame
visual axis opacification (VAO), PCO, membranectomy rates for significant VAOTimepoint: one year—

Secondary

MeasureTime frame
NILTimepoint: NIL—

Countries

India

Contacts

Public ContactJagat Ram
drjagatram@yahoo.com01722756111

Outcome results

None listed

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