Aphakia Versus Pseudophakia in Children Under 2 Years Undergoing Bilateral Congenital Cataract Surgery

Sponsor
Iladevi Cataract and IOL Research Center (Other)
Overall Status
Completed
CT.gov ID
NCT01297153
Collaborator
(none)
100
1
2
96
1

Study Details

Study Description

Brief Summary

The purpose of this study is to document the safety and efficacy of primary IOL implantation in children below 2 years of age undergoing congenital cataract surgery.

Condition or Disease Intervention/Treatment Phase
  • Device: Intraocular Lens (Acrysof IOL)
  • Device: No IOL
Phase 4

Detailed Description

The use of IOLs in pediatric patients has become increasingly popular in recent years and may represent a standard of care for older children. The refinements in surgical techniques attained in adult cataract surgery have been translated to pediatric cataract surgery to produce a technically safe eye. Nevertheless, the use of IOLs in children younger than 2 years remains controversial. Exaggerated inflammation, capsular opacification and changing refractive status of the developing eye should be considered before the use of IOLs in the first two years of life. Further more, there is concern about the unknown risks of an IOL over the long life span.

Currently, there are 3 methods of optical rehabilitation following congenital cataract surgery :

  1. Primary IOL implantation.

  2. Aphakic glasses.

  3. Contact lenses.

At present, there is no randomized clinical trial reported to document the safety and efficacy of IOL implantation in children less than 2 years.

Aim : To compare the technical outcome (safety) and functional outcome (benefits) following primary IOL implantation and aphakia in children less than 2 years.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
100 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Aphakia vs Pseudophakia - Randomized Clinical Trial in Children Under 2 Years Undergoing Bilateral Congenital Cataract Surgery
Study Start Date :
May 1, 2003
Actual Primary Completion Date :
Jan 1, 2011
Actual Study Completion Date :
May 1, 2011

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Aphakia

The patient is randomly assigned for aphakia / pseudophakia. This is done only after vitrectomy. If it is aphakia,IOL will not be implanted.Aphakia will be corrected with aphakic glasses / contact lenses. Bilateral aphakes are given both contact lenses and glasses. So when they do not wear contact lenses they can put on aphakic glasses. Unilateral aphakes are given only contact lenses. Contact lenses should be fitted in the eye in OT immediately after the operation. Aphakic glasses : Prescribed within 2 weeks of surgery for both eyes.

Device: No IOL
No IOL will be implanted in these eyes

Active Comparator: Pseudophakia

The patient is randomly assigned for aphakia / pseudophakia. This is done only after vitrectomy. Hydrophobic Acrysof IOL is implanted.All pseudophakic children will be refracted and given the residual correction within a month of surgery.

Device: Intraocular Lens (Acrysof IOL)
IOL fixation, material and size are important determinants of immediate and long-term outcome. In-the-bag fixation is the most preferred site of IOL implantation.
Other Names:
  • Hydrophobic Acrylic IOL
  • Outcome Measures

    Primary Outcome Measures

    1. Visual axis obscuration [4 years]

      Visual axis obscuration(VAO) assesed on slitlamp or under operating microscope in dilated pupil.VAO is defined as fibrous or proliferative cell growth leadind to a dull retinoscopic reflex.

    2. Glaucoma [4 years]

      Intraocular pressure (IOP) measured with Perkins handheld applanation tonometer. Glaucoma defined as : IOP>21 mmHg >1 occasion with any of these 3 criteria Optic nerve cupping asymmetry >0.2 cd ratio asymmetry , CD ratio >0.4 Abnormal asymmetrical axial length elongation Corneal oedema or enlargement

    3. Central Corneal Thickness [4 Years]

      Corneal thickness assessed by ultrasonic pachymetry. An average of 3 values with an error less than 0.001 would be taken into account.

    Secondary Outcome Measures

    1. Visual Acuity [4 years .]

      An Objective visual assessment to be performed using Lea Grating Paddles(Grating Acuity Test developed by Lea Hyvarinen16), Cardiff Acuity Cards(Preferential Looking Test17), or ETDRS (Early Treatment of Diabetic Retinopathy Study) chart. Vision is subjectively assessed as the ability to follow or to fixate on a point source of light or on an object shown to the child.. Ocular alignment was measured using alternative cover testing. If this kind of testing was not feasible, Hirschberg testing was performed..

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    N/A to 24 Months
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Children less than 2 years

    • Congenital cataract

    • Bilateral cataracts

    • IOL fixation - Bag/Ciliary fixated

    Exclusion Criteria:
    • Microphthalmos (Mean axial length 2 SDs less than normal for age)

    • Microcornea (Horizontal corneal diameter <9.5 mm-asper that particular age)

    • Iris coloboma

    • PHPV

    • Aniridia

    • *Glaucoma - IOP more than or equal to 25 mmHg

    • One eyed

    • Cataract surgery already performed in fellow eye

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Iladevi Cataract & IOL Research Centre Ahmedabad India

    Sponsors and Collaborators

    • Iladevi Cataract and IOL Research Center

    Investigators

    • Principal Investigator: Abhay R Vasavada, MS,FRCS, Iladevi Cataract And IOL Research Centre

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    , ,
    ClinicalTrials.gov Identifier:
    NCT01297153
    Other Study ID Numbers:
    • icircAP
    First Posted:
    Feb 16, 2011
    Last Update Posted:
    Jul 1, 2011
    Last Verified:
    Jun 1, 2011

    Study Results

    No Results Posted as of Jul 1, 2011