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TerminatedNCT03409185Updated Dec 8, 2023

The Incidence of Glistenings in the 2017 Intraocular Lenses Made by Alcon and Abbott Medical Optics

An interventional study of Alcon 1 piece SA60AT lens and AMO 1-piece AABOO lens in Cataracts, Visual Acuity Reduced Transiently and Loss of Visual Contrast Sensitivity, sponsored by University of Toronto. Terminated at 1 site in Canada. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2023-12-08.

Sponsored by University of Toronto · Not applicable, Interventional, and Treatment

Why this study was terminated
The study was terminated because of low recruitment/enrolment due to multiple reasons, including 1) Elderly population, often with other health issues, thus not being able to commit to all of the follow-up appointments and 2) COVID-19 restrictions.
Phase
Not applicable
Study type
Interventional
Enrollment
22
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

The purpose of this study is to seek academic/non-industry research funding support to independently investigate the incidence and density of lens glistenings in cataract patients who are implanted with the latest generations of intraocular lenses (IOL) manufactured by Alcon and AMO Medical Optics.

Read the detailed description

Glistenings are tiny, clear sparkling, fluid-filled microvacuoles that form within a lens after it has been placed in the eye. Glistenings are seen in all lenses but certain lenses develop a higher number of glistenings than others. The effect of glistenings on patients' visual functioning is largely unknown.

The occurrence of glistenings is in part related to the manufacturing technique. In 2013, manufacturers have claimed that recent improvements in manufacturing process have reduced the occurrence of glistenings. There is a lack of independent evaluation of this claim. We would like to assess independently: 1) How frequently do glistenings occur in patients implanted with the 2015 generation lenses? 2) Is there a difference in glistening occurrence between lenses manufactured by Alcon and Abbott Medical Optics (AMO) - the two largest companies in eye care products?

Two-hundred and seventy-six patients will be randomly assigned to receive Alcon or AMO lenses for their cataract surgery at the Kensington Eye Institute (KEI). After surgery, patients will be instructed to return for follow-up visits at 1 month, 6 months, 12 months and 18 months to assess for the occurrence of glistenings. If glistenings are observed at an earlier follow-up visit (e.g., the 6 month visit), patients will still be instructed to come for future visits so that changes in the glistenings over time can be observed.

Project Time-line:

Months 1-8: Participants recruiting, surgical operations, follow-up visits. Months 9-24: follow-up visits, data entry, cleaning and analysis, early results presentation, manuscript preparation and final report.

02

Conditions studied

  • Cataracts
  • Visual Acuity Reduced Transiently
  • Loss of Visual Contrast Sensitivity
  • Functional Visual Loss

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Keywords

  • Cataract surgery
  • Intraocular lens
  • Glistenings
03

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Patients consulting 5 surgeons for cataract surgery in the surgeon's primary offices
  • Patients aged 18 years or older
  • Patients who signed the consent form

Exclusion criteria

Exclusion Criteria:

  • Individuals who cannot understand English in either written or verbal form and do not have language assistance available (e.g. from family members, friends)
  • Patients with co-existing condition of corneal disease
  • Patients with co-existing condition of uveitis
  • Patients with co-existing condition of optic nerve disease
  • Patients with co-existing condition of macular disease
  • Patients with co-existing condition of diabetes
  • Patients with co-existing condition of severe glaucoma (i.e. C/D ratio >=0.9 AND the patient is on glaucoma treatment)
  • Patients with prior refractive surgery
  • Patients with complications of cataract surgery occurred during or after surgery
04

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
22 participants (actual)

Study arms

  • Experimental
    Alcon lens group

    Alcon 1 piece SA60AT lens

    Device: Alcon 1 piece SA60AT lens

  • Active comparator
    AMO lens group

    AMO 1 piece Sensar AABOO lens

    Device: AMO 1-piece AABOO lens

Interventions

  • DeviceAlcon 1 piece SA60AT lens

    Optic Diameter: 6.0 mm, Overall length: 13.0 mm, Material: Ultraviolet-absorbing Acrylate/Methacrylate Copolymer

  • DeviceAMO 1-piece AABOO lens

    Optic Diameter: 6.0 mm, Overall length: 13.0 mm, Material: Ultraviolet-blocking hydrophobic acrylic

05

What researchers measure

Primary outcomes

  1. Incidence and density (severity) of glistenings at 18-month follow-up visit

    To determine if glistenings develop, eyes are dilated and examined. Photographs of the IOLs will be taken with a slit lamp camera for documentation. These photographs will then be assessed for glistenings in two ways: first by trained ophthalmology staff, and second using the ImageJ software Glistenings will be counted and graded on a scale of 0 to 5+ as following: 0. No glistening 1. Less than 10 glistenings 2. 10 to 25 glistenings 3. 25 to 50 glistenings 4. 50 to 100 glistenings 5. Greater than 100 glistenings

    Time frame: 18-month follow-up

Secondary outcomes

  1. Visual acuity in eyes with glistenings at 18-month follow-up visit

    Best corrected visual acuity: acuteness/clearness of vision. This will be tested with the ETDRS (early treatment diabetic retinopathy study) chart.

    Time frame: 18 month follow-up

  2. Contrast sensitivity in eyes with glistenings at 18-month follow-up visit

    Contrast sensitivity: the ability of the visual system to distinguish between an object and its background. This will be tested with the Vector Vision CSV-1000HGT.

    Time frame: 18 month follow-up

  3. Glare disability in eyes with glistenings at 18-month follow-up visit

    Glare disability: the difficulty seeing in the presence of very bright light such as night-time lighting or sunshine. This will be tested using the Brightness Acuity Tester (BAT).

    Time frame: 18 month follow-up

  4. Visual acuity in eyes with glistenings at 12-month follow-up visit

    Best corrected visual acuity: acuteness/clearness of vision. This will be tested with the ETDRS (early treatment diabetic retinopathy study) chart

    Time frame: 12-month follow-up

  5. Contrast sensitivity and glare disability in eyes with glistenings at 12-month follow-up visit

    Contrast sensitivity: the ability of the visual system to distinguish between an object and its background. This will be tested with the Vector Vision CSV-1000HGT.

    Time frame: 12-month follow-up

  6. Glare disability in eyes with glistenings at 12-month follow-up visit

    Glare disability: the difficulty seeing in the presence of very bright light such as night-time lighting or sunshine. This will be tested using the Brightness Acuity Tester (BAT).

    Time frame: 12-month follow-up

  7. Visual acuity in eyes with glistenings at 6-month follow-up visit

    Best corrected visual acuity: acuteness/clearness of vision. This will be tested with the ETDRS (early treatment diabetic retinopathy study) chart.

    Time frame: 6-month follow-up

  8. Contrast sensitivity in eyes with glistenings at 6-month follow-up visit

    Contrast sensitivity: the ability of the visual system to distinguish between an object and its background. This will be tested with the Vector Vision CSV-1000HGT.

    Time frame: 6-month follow-up

  9. Glare disability in eyes with glistenings at 6-month follow-up visit

    Glare disability: the difficulty seeing in the presence of very bright light such as night-time lighting or sunshine. This will be tested using the Brightness Acuity Tester (BAT).

    Time frame: 6-month follow-up

  10. Incidence of glistenings at 12-month follow-up visit

    To determine if glistenings develop, eyes are dilated and examined. Photographs of the IOLs will be taken with a slit lamp camera for documentation. These photographs will then be assessed for glistenings in two ways: first by trained ophthalmology staff, and second using the ImageJ software Glistenings will be counted and graded on a scale of 0 to 5+ as following: 0. No glistening 1. Less than 10 glistenings 2. 10 to 25 glistenings 3. 25 to 50 glistenings 4. 50 to 100 glistenings 5. Greater than 100 glistenings

    Time frame: 12-month follow-up

  11. Incidence of glistenings at 6-month follow-up visit

    To determine if glistenings develop, eyes are dilated and examined. Photographs of the IOLs will be taken with a slit lamp camera for documentation. These photographs will then be assessed for glistenings in two ways: first by trained ophthalmology staff, and second using the ImageJ software Glistenings will be counted and graded on a scale of 0 to 5+ as following: 0. No glistening 1. Less than 10 glistenings 2. 10 to 25 glistenings 3. 25 to 50 glistenings 4. 50 to 100 glistenings 5. Greater than 100 glistenings

    Time frame: 6-month follow-up

06

Study locations

1 site
  • Kensington Eye Institute
    Toronto, Ontario M5T3A9, Canada
07

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

08

Registry details

Key details

Study ID
NCT03409185
Lead sponsor
University of Toronto
Collaborators
Kensington Eye Institute
Responsible party
Yaping Jin (Associate Professor in Ophthalmic Epidemiology, University of Toronto) — Principal investigator
First posted
Jan 24, 2018
Start date
Jul 11, 2017
Primary completion
Mar 31, 2023
Completion
Mar 31, 2023
Last update
Dec 8, 2023

Study contacts

Sherif El-Defrawy, MD, FRCSC
principal investigator · University of Toronto
Yaping Jin, MD, PhD
principal investigator · University of Toronto

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
Yes
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