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Comparison of AmblyzTM Glasses and Patching for Amblyopia

Primary Purpose

Amblyopia

Status
Terminated
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
4-hour AmblyZ glasses
12-hour AmblyZ glasses
2-hour patching
6-hour patching
Sponsored by
Indiana University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Amblyopia focused on measuring amblyopia

Eligibility Criteria

3 Years - 8 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Both genders and all races are eligible to this study.
  • Age 3 to 8 years
  • Amblyopia associated with strabismus, anisometropia, or both
  • Visual acuity in the amblyopic eye between 20/40 and 20/80 inclusive
  • Visual acuity in the sound eye 20/40 or better and inter-eye acuity difference >3 logarithm of the minimum angle of resolution (logMAR) lines
  • Wearing of optimal spectacle correction for a minimum of 4 weeks at the time of enrollment.

Exclusion Criteria:

• No amblyopia treatment before enrollment.

Sites / Locations

  • Riley Hospital for Children

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Active Comparator

Experimental

Active Comparator

Arm Label

4-hour AmblyZ glasses

2-hour eye patching

12-hour AmblyZ glasses

6-hour eye patching

Arm Description

4-hour AmblyZ glasses for moderate amblyopia

2-hour eye patching for moderate amblyopia

12-hour AmblyZ glasses for severe amblyopia

6-hour eye patching for severe amblyopia

Outcomes

Primary Outcome Measures

Visual Acuity Change During 12 Weeks
Visual acuity change during 12 weeks: the difference of visual acuity at baseline and 12 weeks.

Secondary Outcome Measures

Full Information

First Posted
October 25, 2013
Last Updated
July 25, 2017
Sponsor
Indiana University
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1. Study Identification

Unique Protocol Identification Number
NCT01973348
Brief Title
Comparison of AmblyzTM Glasses and Patching for Amblyopia
Official Title
Comparison of AmblyzTM Glasses and Patching for Amblyopia
Study Type
Interventional

2. Study Status

Record Verification Date
July 2017
Overall Recruitment Status
Terminated
Why Stopped
funding and personnel are lack.
Study Start Date
November 2013 (undefined)
Primary Completion Date
May 2016 (Actual)
Study Completion Date
May 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Indiana University

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Electronic eyeglasses, Amblyz™glasses, are a new medical device designed to treat amblyopia, which intermittently become opaque and provide effective occlusion for 50% of the time they are worn. A non-randomized study reported that Amblyz glasses yield an improvement in the amblyopic eye and offer an alternative effective treatment. We are unaware of any randomized clinical trial reports of response to AmblyzTM glasses treatment of amblyopia. Our hypothesis: Amblyz™glasses can improve visual acuity of the amblyopic eye as effective as traditional patching treatment. The primary objective is to determine if AmblyzTM equally treats moderate amblyopia as the standard 2-hour patching treatment and AmblyzTM equally treats severe amblyopia as the standard 6-hour patching treatment. This study is designed to evaluate the effectiveness of a novel amblyopia treatment, AmblyzTM glasses, in treating amblyopia. Moderate amblyopia: Children ages 3 to <8 years with visual acuity of 20/40 to 20/80 in the amblyopic eye will be enrolled and randomized into two groups: 4-hour AmblyzTM glasses treatment group and standard 2-hour patching control group. Severe amblyopia: Children ages 3 to <8 years with visual acuity of 20/100 to 20/400 in the amblyopic eye will be enrolled and randomized into two groups: 12-hour AmblyzTM glasses treatment group and standard 6-hour patching control group.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Amblyopia
Keywords
amblyopia

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
45 (Actual)

8. Arms, Groups, and Interventions

Arm Title
4-hour AmblyZ glasses
Arm Type
Experimental
Arm Description
4-hour AmblyZ glasses for moderate amblyopia
Arm Title
2-hour eye patching
Arm Type
Active Comparator
Arm Description
2-hour eye patching for moderate amblyopia
Arm Title
12-hour AmblyZ glasses
Arm Type
Experimental
Arm Description
12-hour AmblyZ glasses for severe amblyopia
Arm Title
6-hour eye patching
Arm Type
Active Comparator
Arm Description
6-hour eye patching for severe amblyopia
Intervention Type
Device
Intervention Name(s)
4-hour AmblyZ glasses
Intervention Description
4-hour AmblyZ glasses for moderate amblyopia
Intervention Type
Device
Intervention Name(s)
12-hour AmblyZ glasses
Intervention Description
12-hour AmblyZ glasses for severe amblyopia
Intervention Type
Device
Intervention Name(s)
2-hour patching
Intervention Description
2-hour patching for moderate amblyopia
Intervention Type
Device
Intervention Name(s)
6-hour patching
Intervention Description
6-hour patching for severe amblyopia
Primary Outcome Measure Information:
Title
Visual Acuity Change During 12 Weeks
Description
Visual acuity change during 12 weeks: the difference of visual acuity at baseline and 12 weeks.
Time Frame
12 weeks
Other Pre-specified Outcome Measures:
Title
Reverse Amblyopia
Description
it is defined that the strong eye of the patient decreases two logMAR lines over 3 months.
Time Frame
3 Months
Title
Significant Ocular Deviation Increase From the Baseline
Description
The significant ocular deviation is defined as equal or over 10 degrees of deviation more than that of the baseline.
Time Frame
3 Months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
3 Years
Maximum Age & Unit of Time
8 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Both genders and all races are eligible to this study. Age 3 to 8 years Amblyopia associated with strabismus, anisometropia, or both Visual acuity in the amblyopic eye between 20/40 and 20/80 inclusive Visual acuity in the sound eye 20/40 or better and inter-eye acuity difference >3 logarithm of the minimum angle of resolution (logMAR) lines Wearing of optimal spectacle correction for a minimum of 4 weeks at the time of enrollment. Exclusion Criteria: • No amblyopia treatment before enrollment.
Facility Information:
Facility Name
Riley Hospital for Children
City
Indianapolis
State/Province
Indiana
ZIP/Postal Code
46202
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
27418249
Citation
Wang J, Neely DE, Galli J, Schliesser J, Graves A, Damarjian TG, Kovarik J, Bowsher J, Smith HA, Donaldson D, Haider KM, Roberts GJ, Sprunger DT, Plager DA. A pilot randomized clinical trial of intermittent occlusion therapy liquid crystal glasses versus traditional patching for treatment of moderate unilateral amblyopia. J AAPOS. 2016 Aug;20(4):326-31. doi: 10.1016/j.jaapos.2016.05.014. Epub 2016 Jul 12.
Results Reference
derived

Learn more about this trial

Comparison of AmblyzTM Glasses and Patching for Amblyopia

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