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OpenTrials
Completed

NCT Number: NCT00756327

AquaLase Capsule Wash for Pediatric Eyes

To determine whether AquaLase capsule wash reduces posterior capsule opacification (PCO) in pediatric eyes.

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Key information

Age range

6 year–15 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Aravind Haripriya

Madurai, India

About this study

Dramatic advances have occurred in the treatment of childhood cataracts in the last 10 years. Intraocular lens (IOL) implantation has been universally accepted as the standard of care for most children undergoing cataract surgery beyond infancy. Despite advances in cataract surgery in children, PCO remained a significant complication following pediatric cataract surgery. In addition to being visually disturbing, it also induces amblyopia in children and if not treated at the earliest, irreversible visual changes may occur. The younger the child, the more acute is the problem: PCO occurs faster and the effect of amblyopia is more pronounced.

To prevent opacification of the visual axis after cataract surgery, primary posterior capsulectomy and vitrectomy are routinely needed while managing pediatric cataract. This surgical step is not routinely used in adult cataract surgery, where we prefer an intact posterior capsule. Researchers are constantly trying to find a way to avoid the need for invasive procedures like posterior capsulectomy and vitrectomy for pediatric eyes. Use of AquaLase technology has shown some capability in cleaning the capsular bag during cataract surgery. Observations of this include anecdotal observation from users. AquaLase for cataract removal with the Infiniti Vision System has been used since 2003, is registered, and the FDA clearance is 510(k) number K980292. AquaLase uses pulses of warmed balanced salt solution to gently emulsify and facilitate aspiration of cataracts. The device under evaluation falls under the same FDA clearance. The unique aspect is the application tip which is intended to allow more thorough capsular bag cleaning or removal of more residual lens material than is currently being achieved. The energy source, controls, and materials are all identical to the currently marketed product. The difference is in the geometry of the distal most end of the application tip.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Bilateral cataract in a child aged 6-15 years old
  • Informed consent from the parents/legal guardian.

Exclusion criteria

  • traumatic cataract
  • fellow eye - visually not significant cataract
  • fellow eye surgery not scheduled within 3-month period after first eye surgery
  • dense posterior capsule plaque
  • preexisting posterior capsule defect
  • subluxated cataract
  • high myopia (defined as axial length >24 mm)
  • child with multiple disability where it may not be feasible to perform YAG laser capsulotomy in the office, if needed
  • Participants with a strong likelihood of non-adherence (difficulties in adhering to follow-up schedule due to geographic distance from clinical center)

Sponsors and collaborators

Lead sponsor

Medical University of South Carolina

Other

Collaborators

  • Alcon Research

Registry information

Important dates

Study start
2007
Primary completion
2009
Study completion
2009
First posted
Sep 22, 2008
Registry last updated
Aug 17, 2009

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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