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Trial Comparing Patching With Active Vision Therapy to Patching With Control Vision Therapy as Treatment for Amblyopia

A Randomized Trial Comparing Patching With Active Vision Therapy to Patching With Control Vision Therapy as Treatment for Amblyopia in Children 7 to <13 Years Old

Status
Terminated
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00587171
Acronym
ATS12
Enrollment
19
Registered
2008-01-07
Start date
2008-04-30
Completion date
2009-10-31
Last updated
2016-07-13

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

Conditions

Amblyopia

Keywords

Amblyopia, Vision Therapy, Patching

Brief summary

This study is comparing the effectiveness of patching combined with active vision therapy plus near activities versus patching combined with control vision therapy plus near activities for moderate amblyopia (20/40-20/100) in 7 to \<13 year olds. The primary outcome measure is the proportion of patients with visual acuity of 20/25 or better in the amblyopic eye at the 17-week masked exam. These patients will be considered treatment responders. The primary analysis will consist of a comparison between the 2 treatment groups of the proportion of treatment responders with adjustment for baseline visual acuity. Secondary outcomes are stereoacuity at the 17-week masked exam, mean improvement in visual acuity at the 17-week masked exam, and rate of improvement of visual acuity.

Detailed description

Patching and atropine have been traditionally used for the improvement of visual acuity in children with amblyopia. Previous studies have shown that these methods of treatment are effective in young children with functional amblyopia. More recently ATS3, a randomized clinical trial of 507 children ages 7-\<18, found that part-time patching combined with atropine and near activities improved visual acuity by two or more lines in 53% of the 7 to 12 year olds compared to 25% for optical correction alone. For the 13 to 17 year olds, part-time patching and near activities improved visual acuity by 2 or more lines in 25%, compared to 23% for optical correction alone. While it appears that patching and/or atropine, combined with near activities, can improve visual acuity in some patients ages 7-\<18, most patients in the study were left with residual visual acuity deficits. To further improve visual acuity and binocularity in children with amblyopia some eye care providers augment these traditional therapies with vision therapy. Vision therapy is prescribed initially if there is moderate amblyopia with stereopsis. Vision therapy can be added to the treatment regimen once the patient has reached moderate levels of vision loss with stereopsis and if the patient is still not responding to the current treatment and still has moderate amblyopia. It is thought that the best candidates for this type of therapy are those children with a minimum level of stereopsis (at least 800) and without constant strabismus. Those children with no stereopsis would not be able to perform the activities in the later stages of therapy utilizing binocular vision. Vision therapy is a sequence of prescribed activities typically performed on a daily basis at home and weekly in-office, and is directed toward an individual patient's deficient skills. Visual skills are practiced under conditions that provide the patient with feedback. The feedback, along with a gradual increase in the demand of the activities as improvement occurs, enables the patient to improve visual functions such as visual acuity, fixation, accommodation, and vergence skills. There have been case reports and small sample studies that have shown that vision therapy in combination with spectacles and occlusion is effective in improving the visual acuity of patients with amblyopia. Wick et al looked at nineteen patients who were diagnosed with anisometropic amblyopia between the ages of 6 to 49. Seventeen of the patients had moderate amblyopia and two had severe amblyopia, based on the definition of amblyopia used in the Amblyopia Treatment Studies. The patients were treated with a sequence that included spectacle correction, occlusion therapy and both monocular and binocular vision therapy. Thirteen of the seventeen patients with moderate amblyopia had a final visual acuity of 20/25 or better and all of the patients with moderate amblyopia had 20/30 or better final visual acuity. More recent reports on perceptual learning, an active form of therapy in which amblyopic subjects practice a position-discrimination task, have shown a mean acuity improvement of approximately 30% (two lines) in amblyopic children and adults who had completed occlusion therapy. These studies provide support for the notion that the practice of particular visual skills under conditions that provide the patient with feedback (e.g., vision therapy) may be beneficial in improving the visual performance of amblyopic eyes. The second reason to prescribe active therapy is to enhance or facilitate the effects of occlusion by directly treating the aforementioned deficits found to be associated with amblyopia. Most therapy procedures are designed to remediate specific deficiencies in four main areas: fixation, spatial perception, accommodative efficiency, binocular function and oculomotor control. Lastly, some investigators have suggested that the use of vision therapy may reduce the likelihood of recurrence of the amblyopia. This may be particularly true with anisometropic amblyopia in which vision therapy can be used to improve binocular function.

Interventions

DEVICEPatching

2 hours daily patching

30 minutes daily near activities at home

PROCEDUREActive vision therapy

30 minutes of daily at-home active vision therapy and a weekly 45 minute in-office active vision therapy session

PROCEDUREControl vision therapy

30 minutes of daily at-home control vision therapy and a weekly 45 minute in-office control vision therapy session

Sponsors

National Eye Institute (NEI)
CollaboratorNIH
Jaeb Center for Health Research
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
7 Years to 12 Years
Healthy volunteers
No

Inclusion criteria

* Age 7 to \<13 years * Amblyopia associated with anisometropia, strabismus (comitant or incomitant), or both at the time of the eligibility examination * Visual acuity in the amblyopic eye between 49 and 71 letters inclusive (20/40 to 20/100 inclusive) on the eETDRS * Visual acuity in the sound eye of 79 or more letters on the eETDRS (20/25 or better) * Inter-eye acuity difference of 15 or more letters (3 or more logMAR lines) * At least 800 seconds of arc on the Randot Preschool Stereoacuity Test * Previous or current amblyopia treatment with spectacles or contact lenses, patching or atropine is permitted. * No myopia more than -6.00 D spherical equivalent in the amblyopic eye * Single vision spectacles, if needed, worn for at least 16 weeks or until visual acuity documented to be stable * The child has access to a computer on a daily basis (to use the home vision therapy software)

Exclusion criteria

* Previous vision therapy or orthoptics * Known skin reactions to patch or bandage adhesives * Prior intraocular or refractive surgery * Bifocals * Constant strabismus at near at the eligibility examination * A family member is (or has been) enrolled in this study

Design outcomes

Primary

MeasureTime frameDescription
Distribution of Distance Visual Acuity in Amblyopic Eye at 17-week Outcome17 weeksVisual acuity was measured with the electronic early treatment diabetic retinopathy (E-ETDRS) method and resulted in a letter score that could range from 0 to 97 letters, with 0 being the worst and 97 being the best.
Mean (SD): Distance Visual Acuity in Amblyopic Eye at 17-week Outcome17 weeksVisual acuity was measured with the electronic early treatment diabetic retinopathy (E-ETDRS) method and resulted in a letter score that could range from 0 to 97 letters, with 0 being the worst and 97 being the best.
Distribution of Change in Amblyopic Eye Visual Acuity From Baseline to 17 WeeksBaseline to 17 weeksVisual acuity was measured with the electronic early treatment diabetic retinopathy (E-ETDRS) method and resulted in a letter score that could range from 0 to 97 letters, with 0 being the worst and 97 being the best. A difference was calculated as the difference in letters between baseline and outcome with positive difference indicating improvement in acuity.
Mean (SD) of Change in Amblyopic Eye Visual Acuity From Baseline to 17 WeeksBaseline to 17 weeksVisual acuity was measured with the electronic early treatment diabetic retinopathy (E-ETDRS) method and resulted in a letter score that could range from 0 to 97 letters, with 0 being the worst and 97 being the best. A difference was calculated as the difference in letters between baseline and outcome with positive difference indicating improvement in acuity.

Secondary

MeasureTime frameDescription
Mean (SD) of Intereye Visual Acuity at 17 Weeks17 weeksVisual acuity was measured with the electronic early treatment diabetic retinopathy (E-ETDRS) method and resulted in a letter score that could range from 0 to 97 letters, with 0 being the worst and 97 being the best.
Mean (SD) of Change in Intereye Visual Acuity From Baseline to 17 WeeksBaseline to 17 weeksVisual acuity was measured with the electronic early treatment diabetic retinopathy (E-ETDRS) method and resulted in a letter score that could range from 0 to 97 letters, with 0 being the worst and 97 being the best. A difference was calculated as the difference in letters between baseline and outcome with positive difference indicating improvement in acuity.
Distribution of Fellow Eye Visual Acuity at 17 Weeks17 weeksVisual acuity was measured with the electronic early treatment diabetic retinopathy (E-ETDRS) method and resulted in a letter score that could range from 0 to 97 letters, with 0 being the worst and 97 being the best.
Distribution of Change in Randot Preschool Steroacuity From Baseline to 17 WeeksBaseline to 17 weeksThe Randot Preschool Stereotest measures stereopsis from 800 to 40 seconds of arc on patients as young as 2 years of age. This Stereotest is designed as a matching game in which the patient matches pictures in a test booklet wearing special glasses. A subject can fail the pretest (not see any pictures) or can score \>800 (the worst), 800, 400, 200, 100, 60, or 40 (the best) seconds of arc. If two shapes are identified correctly the patient progresses to the next lower stereoacuity level. A failed test occurs when the patient cannot identify any shapes.
Distribution of Randot Preschool Stereoacuity at 17 Weeks17 weeksThe Randot Preschool Stereotest measures stereopsis from 800 to 40 seconds of arc. This Stereotest is designed as a matching game in which the patient matches pictures in a test booklet wearing special glasses. A subject can fail the pretest (not see any pictures) or can score \>800 (the worst), 800, 400, 200, 100, 60, or 40 (the best) seconds of arc. If two shapes are identified correctly the patient progresses to the next lower stereoacuity level. A failed test occurs when the patient cannot identify any shapes.
Mean (SD) of Fellow Eye Visual Acuity at 17 Weeks17 weeksVisual acuity was measured with the electronic early treatment diabetic retinopathy (E-ETDRS) method and resulted in a letter score that could range from 0 to 97 letters, with 0 being the worst and 97 being the best.
Distribution of Change in Fellow Eye Visual Acuity From Baseline to 17 WeeksBaseline to 17 weeksVisual acuity was measured with the electronic early treatment diabetic retinopathy (E-ETDRS) method and resulted in a letter score that could range from 0 to 97 letters, with 0 being the worst and 97 being the best. A difference was calculated as the difference in letters between baseline and outcome with positive difference indicating improvement in acuity.
Mean (SD) of Change in Fellow Eye Visual Acuity From Baseline to 17 WeeksBaseline to 17 weeksVisual acuity was measured with the electronic early treatment diabetic retinopathy (E-ETDRS) method and resulted in a letter score that could range from 0 to 97 letters, with 0 being the worst and 97 being the best. A difference was calculated as the difference in letters between baseline and outcome with positive difference indicating improvement in acuity.

Countries

United States

Participant flow

Recruitment details

Nineteen subjects were recruited by 7 community based or institutional based sites between April 2008 and March 2009.

Pre-assignment details

At enrollment, subjects were required to have been treated with at least 16 weeks of single vision spectacles (if needed) or until visual acuity was documented to be stable. The child must have had access to a computer on a daily basis.

Participants by arm

ArmCount
Active
2 hours of daily patching combined with 1 hour daily of near activities (that includes 30 minutes of at-home active vision therapy) and weekly in-office active vision therapy
9
Control
2 hours of daily patching combined with 1 hour of daily near activities (that includes 30 minutes of at-home control vision therapy) and weekly in-office control vision therapy
10
Total19

Withdrawals & dropouts

PeriodReasonFG000FG001
Overall StudyLost to Follow-up11

Baseline characteristics

CharacteristicActiveControlTotal
Age, Continuous10.1 years
STANDARD_DEVIATION 2.1
10.0 years
STANDARD_DEVIATION 1.8
10.0 years
STANDARD_DEVIATION 1.9
Age, Customized
10 years old
1 participants0 participants1 participants
Age, Customized
11 years old
0 participants4 participants4 participants
Age, Customized
12 years old
3 participants1 participants4 participants
Age, Customized
7 years old
1 participants2 participants3 participants
Age, Customized
8 years old
2 participants1 participants3 participants
Age, Customized
9 years old
2 participants2 participants4 participants
Cause of Amblyopia
Anisometropia
4 participants5 participants9 participants
Cause of Amblyopia
Strabismus
0 participants2 participants2 participants
Cause of Amblyopia
Strabismus and anisometropia
5 participants3 participants8 participants
Distance visual acuity in amblyopic eye
20/100 (48 to 52 letters) (worse)
2 participants2 participants4 participants
Distance visual acuity in amblyopic eye
20/40 (68 to 72 letters) (best)
2 participants4 participants6 participants
Distance visual acuity in amblyopic eye
20/50 (63 to 67 letters)
4 participants2 participants6 participants
Distance visual acuity in amblyopic eye
20/63 (58 to 62 letters)
1 participants1 participants2 participants
Distance visual acuity in amblyopic eye
20/80 (53 to 57 letters)
0 participants1 participants1 participants
Distance visual acuity in fellow eye
20/16 (88 to 92 letters) (best)
3 participants3 participants6 participants
Distance visual acuity in fellow eye
20/20 (83 to 87 letters)
4 participants5 participants9 participants
Distance visual acuity in fellow eye
20/25 (78 to 82 letters)
2 participants2 participants4 participants
Distance visual acuity in fellow eye
20/32 (73 to 77 letters)
0 participants0 participants0 participants
Distance visual acuity in fellow eye
20/40 (68 to 72 letters) (worse)
0 participants0 participants0 participants
Mean (SD) Distance Visual Acuity in Amblyopic Eye62.3 letters
STANDARD_DEVIATION 6.8
61.9 letters
STANDARD_DEVIATION 7.9
62.1 letters
STANDARD_DEVIATION 7.2
Mean (SD) Distance Visual Acuity in Fellow Eye85.3 letters
STANDARD_DEVIATION 3.6
86.2 letters
STANDARD_DEVIATION 4
85.8 letters
STANDARD_DEVIATION 3.8
Mean (SD) Intereye Acuity Difference23.0 letters
STANDARD_DEVIATION 6.5
24.3 letters
STANDARD_DEVIATION 8.8
23.7 letters
STANDARD_DEVIATION 7.6
Race/Ethnicity, Customized
Black/African American
0 participants1 participants1 participants
Race/Ethnicity, Customized
Hispanic
6 participants4 participants10 participants
Race/Ethnicity, Customized
White
3 participants5 participants8 participants
Randot Preschool stereoacuity
100 arcsec
2 participants4 participants6 participants
Randot Preschool stereoacuity
200 arcsec
3 participants2 participants5 participants
Randot Preschool stereoacuity
400 arcsec
1 participants2 participants3 participants
Randot Preschool stereoacuity
40 arcsec
0 participants0 participants0 participants
Randot Preschool stereoacuity
60 arcsec
0 participants0 participants0 participants
Randot Preschool stereoacuity
>800 arcsec
0 participants0 participants0 participants
Randot Preschool stereoacuity
800 arcsec
3 participants2 participants5 participants
Randot Preschool stereoacuity
Failed pretest
0 participants0 participants0 participants
Region of Enrollment
United States
9 participants10 participants19 participants
Sex: Female, Male
Female
6 Participants5 Participants11 Participants
Sex: Female, Male
Male
3 Participants5 Participants8 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
— / —— / —
other
Total, other adverse events
0 / 90 / 10
serious
Total, serious adverse events
0 / 90 / 10

Outcome results

Primary

Distribution of Change in Amblyopic Eye Visual Acuity From Baseline to 17 Weeks

Visual acuity was measured with the electronic early treatment diabetic retinopathy (E-ETDRS) method and resulted in a letter score that could range from 0 to 97 letters, with 0 being the worst and 97 being the best. A difference was calculated as the difference in letters between baseline and outcome with positive difference indicating improvement in acuity.

Time frame: Baseline to 17 weeks

ArmMeasureGroupValue (NUMBER)
ActiveDistribution of Change in Amblyopic Eye Visual Acuity From Baseline to 17 Weeks>=1 letter worse0 participants
ActiveDistribution of Change in Amblyopic Eye Visual Acuity From Baseline to 17 Weeks0 letters0 participants
ActiveDistribution of Change in Amblyopic Eye Visual Acuity From Baseline to 17 Weeks1 to 4 letters better0 participants
ActiveDistribution of Change in Amblyopic Eye Visual Acuity From Baseline to 17 Weeks5 to 9 letters better4 participants
ActiveDistribution of Change in Amblyopic Eye Visual Acuity From Baseline to 17 Weeks10 to 14 letters better1 participants
ActiveDistribution of Change in Amblyopic Eye Visual Acuity From Baseline to 17 Weeks>=15 letters better3 participants
ControlDistribution of Change in Amblyopic Eye Visual Acuity From Baseline to 17 Weeks10 to 14 letters better2 participants
ControlDistribution of Change in Amblyopic Eye Visual Acuity From Baseline to 17 Weeks>=1 letter worse0 participants
ControlDistribution of Change in Amblyopic Eye Visual Acuity From Baseline to 17 Weeks5 to 9 letters better4 participants
ControlDistribution of Change in Amblyopic Eye Visual Acuity From Baseline to 17 Weeks0 letters0 participants
ControlDistribution of Change in Amblyopic Eye Visual Acuity From Baseline to 17 Weeks>=15 letters better1 participants
ControlDistribution of Change in Amblyopic Eye Visual Acuity From Baseline to 17 Weeks1 to 4 letters better2 participants
Primary

Distribution of Distance Visual Acuity in Amblyopic Eye at 17-week Outcome

Visual acuity was measured with the electronic early treatment diabetic retinopathy (E-ETDRS) method and resulted in a letter score that could range from 0 to 97 letters, with 0 being the worst and 97 being the best.

Time frame: 17 weeks

ArmMeasureGroupValue (NUMBER)
ActiveDistribution of Distance Visual Acuity in Amblyopic Eye at 17-week Outcome20/50 (63 to 67 letters)0 participants
ActiveDistribution of Distance Visual Acuity in Amblyopic Eye at 17-week Outcome20/32 (73 to 77 letters)0 participants
ActiveDistribution of Distance Visual Acuity in Amblyopic Eye at 17-week Outcome20/63 (58 to 62 letters)1 participants
ActiveDistribution of Distance Visual Acuity in Amblyopic Eye at 17-week Outcome20/25 (78 to 82 letters)2 participants
ActiveDistribution of Distance Visual Acuity in Amblyopic Eye at 17-week Outcome20/40 (68 to 72 letters)3 participants
ActiveDistribution of Distance Visual Acuity in Amblyopic Eye at 17-week Outcome20/20 (83 to 87 letters) (best)2 participants
ActiveDistribution of Distance Visual Acuity in Amblyopic Eye at 17-week Outcome20/80 (53 to 57 letters) (worse)0 participants
ControlDistribution of Distance Visual Acuity in Amblyopic Eye at 17-week Outcome20/20 (83 to 87 letters) (best)1 participants
ControlDistribution of Distance Visual Acuity in Amblyopic Eye at 17-week Outcome20/80 (53 to 57 letters) (worse)1 participants
ControlDistribution of Distance Visual Acuity in Amblyopic Eye at 17-week Outcome20/63 (58 to 62 letters)0 participants
ControlDistribution of Distance Visual Acuity in Amblyopic Eye at 17-week Outcome20/50 (63 to 67 letters)2 participants
ControlDistribution of Distance Visual Acuity in Amblyopic Eye at 17-week Outcome20/40 (68 to 72 letters)1 participants
ControlDistribution of Distance Visual Acuity in Amblyopic Eye at 17-week Outcome20/32 (73 to 77 letters)2 participants
ControlDistribution of Distance Visual Acuity in Amblyopic Eye at 17-week Outcome20/25 (78 to 82 letters)2 participants
Primary

Mean (SD): Distance Visual Acuity in Amblyopic Eye at 17-week Outcome

Visual acuity was measured with the electronic early treatment diabetic retinopathy (E-ETDRS) method and resulted in a letter score that could range from 0 to 97 letters, with 0 being the worst and 97 being the best.

Time frame: 17 weeks

ArmMeasureValue (MEAN)Dispersion
ActiveMean (SD): Distance Visual Acuity in Amblyopic Eye at 17-week Outcome75.6 lettersStandard Deviation 9.7
ControlMean (SD): Distance Visual Acuity in Amblyopic Eye at 17-week Outcome72.0 lettersStandard Deviation 9.6
Primary

Mean (SD) of Change in Amblyopic Eye Visual Acuity From Baseline to 17 Weeks

Visual acuity was measured with the electronic early treatment diabetic retinopathy (E-ETDRS) method and resulted in a letter score that could range from 0 to 97 letters, with 0 being the worst and 97 being the best. A difference was calculated as the difference in letters between baseline and outcome with positive difference indicating improvement in acuity.

Time frame: Baseline to 17 weeks

ArmMeasureValue (MEAN)Dispersion
ActiveMean (SD) of Change in Amblyopic Eye Visual Acuity From Baseline to 17 Weeks12.0 lettersStandard Deviation 5.3
ControlMean (SD) of Change in Amblyopic Eye Visual Acuity From Baseline to 17 Weeks8.8 lettersStandard Deviation 5.3
Secondary

Distribution of Change in Fellow Eye Visual Acuity From Baseline to 17 Weeks

Visual acuity was measured with the electronic early treatment diabetic retinopathy (E-ETDRS) method and resulted in a letter score that could range from 0 to 97 letters, with 0 being the worst and 97 being the best. A difference was calculated as the difference in letters between baseline and outcome with positive difference indicating improvement in acuity.

Time frame: Baseline to 17 weeks

ArmMeasureGroupValue (NUMBER)
ActiveDistribution of Change in Fellow Eye Visual Acuity From Baseline to 17 WeeksWithin 4 letters7 participants
ActiveDistribution of Change in Fellow Eye Visual Acuity From Baseline to 17 Weeks5 to 9 letters better1 participants
ControlDistribution of Change in Fellow Eye Visual Acuity From Baseline to 17 WeeksWithin 4 letters7 participants
ControlDistribution of Change in Fellow Eye Visual Acuity From Baseline to 17 Weeks5 to 9 letters better2 participants
Secondary

Distribution of Change in Randot Preschool Steroacuity From Baseline to 17 Weeks

The Randot Preschool Stereotest measures stereopsis from 800 to 40 seconds of arc on patients as young as 2 years of age. This Stereotest is designed as a matching game in which the patient matches pictures in a test booklet wearing special glasses. A subject can fail the pretest (not see any pictures) or can score \>800 (the worst), 800, 400, 200, 100, 60, or 40 (the best) seconds of arc. If two shapes are identified correctly the patient progresses to the next lower stereoacuity level. A failed test occurs when the patient cannot identify any shapes.

Time frame: Baseline to 17 weeks

ArmMeasureGroupValue (NUMBER)
ActiveDistribution of Change in Randot Preschool Steroacuity From Baseline to 17 Weeks2 or more levels worse1 participants
ActiveDistribution of Change in Randot Preschool Steroacuity From Baseline to 17 WeeksWithin 1 level4 participants
ActiveDistribution of Change in Randot Preschool Steroacuity From Baseline to 17 Weeks2 or more levels better3 participants
ControlDistribution of Change in Randot Preschool Steroacuity From Baseline to 17 Weeks2 or more levels worse2 participants
ControlDistribution of Change in Randot Preschool Steroacuity From Baseline to 17 WeeksWithin 1 level4 participants
ControlDistribution of Change in Randot Preschool Steroacuity From Baseline to 17 Weeks2 or more levels better2 participants
Secondary

Distribution of Fellow Eye Visual Acuity at 17 Weeks

Visual acuity was measured with the electronic early treatment diabetic retinopathy (E-ETDRS) method and resulted in a letter score that could range from 0 to 97 letters, with 0 being the worst and 97 being the best.

Time frame: 17 weeks

ArmMeasureGroupValue (NUMBER)
ActiveDistribution of Fellow Eye Visual Acuity at 17 Weeks20/25 (78 to 82 letters) (worse)2 participants
ActiveDistribution of Fellow Eye Visual Acuity at 17 Weeks20/20 (83 to 87 letters)1 participants
ActiveDistribution of Fellow Eye Visual Acuity at 17 Weeks20/16 (88 to 92 letters)5 participants
ActiveDistribution of Fellow Eye Visual Acuity at 17 Weeks20/12 (93 to 97 letters) (best)0 participants
ControlDistribution of Fellow Eye Visual Acuity at 17 Weeks20/12 (93 to 97 letters) (best)3 participants
ControlDistribution of Fellow Eye Visual Acuity at 17 Weeks20/25 (78 to 82 letters) (worse)0 participants
ControlDistribution of Fellow Eye Visual Acuity at 17 Weeks20/16 (88 to 92 letters)2 participants
ControlDistribution of Fellow Eye Visual Acuity at 17 Weeks20/20 (83 to 87 letters)4 participants
Secondary

Distribution of Randot Preschool Stereoacuity at 17 Weeks

The Randot Preschool Stereotest measures stereopsis from 800 to 40 seconds of arc. This Stereotest is designed as a matching game in which the patient matches pictures in a test booklet wearing special glasses. A subject can fail the pretest (not see any pictures) or can score \>800 (the worst), 800, 400, 200, 100, 60, or 40 (the best) seconds of arc. If two shapes are identified correctly the patient progresses to the next lower stereoacuity level. A failed test occurs when the patient cannot identify any shapes.

Time frame: 17 weeks

ArmMeasureGroupValue (NUMBER)
ActiveDistribution of Randot Preschool Stereoacuity at 17 Weeks40 arcsec (best)2 participants
ActiveDistribution of Randot Preschool Stereoacuity at 17 Weeks60 arcsec1 participants
ActiveDistribution of Randot Preschool Stereoacuity at 17 Weeks100 arcsec2 participants
ActiveDistribution of Randot Preschool Stereoacuity at 17 Weeks200 arcsec0 participants
ActiveDistribution of Randot Preschool Stereoacuity at 17 Weeks400 arcsec2 participants
ActiveDistribution of Randot Preschool Stereoacuity at 17 Weeks800 arcsec1 participants
ActiveDistribution of Randot Preschool Stereoacuity at 17 Weeks>800 arcsec (worse)0 participants
ActiveDistribution of Randot Preschool Stereoacuity at 17 WeeksFailed pretest0 participants
ControlDistribution of Randot Preschool Stereoacuity at 17 WeeksFailed pretest1 participants
ControlDistribution of Randot Preschool Stereoacuity at 17 Weeks40 arcsec (best)1 participants
ControlDistribution of Randot Preschool Stereoacuity at 17 Weeks400 arcsec0 participants
ControlDistribution of Randot Preschool Stereoacuity at 17 Weeks60 arcsec0 participants
ControlDistribution of Randot Preschool Stereoacuity at 17 Weeks>800 arcsec (worse)1 participants
ControlDistribution of Randot Preschool Stereoacuity at 17 Weeks100 arcsec1 participants
ControlDistribution of Randot Preschool Stereoacuity at 17 Weeks800 arcsec1 participants
ControlDistribution of Randot Preschool Stereoacuity at 17 Weeks200 arcsec4 participants
Secondary

Mean (SD) of Change in Fellow Eye Visual Acuity From Baseline to 17 Weeks

Visual acuity was measured with the electronic early treatment diabetic retinopathy (E-ETDRS) method and resulted in a letter score that could range from 0 to 97 letters, with 0 being the worst and 97 being the best. A difference was calculated as the difference in letters between baseline and outcome with positive difference indicating improvement in acuity.

Time frame: Baseline to 17 weeks

ArmMeasureValue (MEAN)Dispersion
ActiveMean (SD) of Change in Fellow Eye Visual Acuity From Baseline to 17 Weeks0.4 lettersStandard Deviation 2.8
ControlMean (SD) of Change in Fellow Eye Visual Acuity From Baseline to 17 Weeks2.9 lettersStandard Deviation 2.7
Secondary

Mean (SD) of Change in Intereye Visual Acuity From Baseline to 17 Weeks

Visual acuity was measured with the electronic early treatment diabetic retinopathy (E-ETDRS) method and resulted in a letter score that could range from 0 to 97 letters, with 0 being the worst and 97 being the best. A difference was calculated as the difference in letters between baseline and outcome with positive difference indicating improvement in acuity.

Time frame: Baseline to 17 weeks

ArmMeasureValue (MEAN)Dispersion
ActiveMean (SD) of Change in Intereye Visual Acuity From Baseline to 17 Weeks11.6 lettersStandard Deviation 4.2
ControlMean (SD) of Change in Intereye Visual Acuity From Baseline to 17 Weeks5.9 lettersStandard Deviation 5
Secondary

Mean (SD) of Fellow Eye Visual Acuity at 17 Weeks

Visual acuity was measured with the electronic early treatment diabetic retinopathy (E-ETDRS) method and resulted in a letter score that could range from 0 to 97 letters, with 0 being the worst and 97 being the best.

Time frame: 17 weeks

ArmMeasureValue (MEAN)Dispersion
ActiveMean (SD) of Fellow Eye Visual Acuity at 17 Weeks86.5 lettersStandard Deviation 4.1
ControlMean (SD) of Fellow Eye Visual Acuity at 17 Weeks89.8 lettersStandard Deviation 3.6
Secondary

Mean (SD) of Intereye Visual Acuity at 17 Weeks

Visual acuity was measured with the electronic early treatment diabetic retinopathy (E-ETDRS) method and resulted in a letter score that could range from 0 to 97 letters, with 0 being the worst and 97 being the best.

Time frame: 17 weeks

ArmMeasureValue (MEAN)Dispersion
ActiveMean (SD) of Intereye Visual Acuity at 17 Weeks10.9 lettersStandard Deviation 9.2
ControlMean (SD) of Intereye Visual Acuity at 17 Weeks17.8 lettersStandard Deviation 9.4

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026