Regimens of Intermittent Occlusion Therapy for Amblyopia in Children

Amblyopia Clinical Trial

Official title:

Intense vs Standard Regimens of Intermittent Occlusion Therapy for Unilateral Moderate Amblyopia in Children

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT02767856
• Other study ID #: HJW1604
• Status: Terminated
• Phase: N/A
• Start date: September 2016
• Est. completion date: May 30, 2021

Study information

• Verified date: May 2022
• Source: Salus University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This study is designed to answer the question: What if the Intermittent Occlusion (IO-therapy) glasses were prescribed all day (12-hours) in which the total time of treatment only took 4 weeks instead of the current treatment time (4 hours) in which it takes 12 weeks? Children aged 3- to 8-years with untreated moderate unilateral amblyopia will be enrolled and randomized into 2 groups: 1) Intense 12-hour IO-therapy Group for 4 weeks treatment; or 2) Standard 4-hour IO-therapy glasses Group for 12 weeks treatment.

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 32
• Est. completion date: May 30, 2021
• Est. primary completion date: May 30, 2021
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 3 Years to 8 Years

Eligibility

Inclusion Criteria:

The following criteria must be met for the patient to be enrolled in the study:

1. Age 3 to < 8 years

2. Unilateral amblyopia associated with strabismus (comitant or incomitant), anisometropia, or both

Criteria for strabismus: At least one of the following criteria must be met:

• Heterotropia at distance and/or near fixation on examination (with or without spectacles)
• History of strabismus surgery
• Documented history of strabismus which is no longer present (which in the judgment of the investigator could have caused amblyopia)

Criteria for anisometropia: At least one of the following criteria must be met:

• >0.50 D difference between eyes in spherical equivalent
• >0.50 D difference between eyes in astigmatism in any meridian

3. Amblyopic eye has no myopia (> -0.25 D spherical equivalent).

4. Visual acuity, measured in each eye without cycloplegia within 7 days prior to

enrollment using the ATS single-surround HOTV letter protocol as follows:

• Visual acuity in the amblyopic eye between 20/40 and 20/80 inclusive
• Visual acuity in the sound eye 20/32 or better
• Inter-eye acuity difference = 2 logMAR lines (i.e., amblyopic eye acuity at least 2 lines worse than sound eye acuity)

5. No previous amblyopia treatment within 6 months.

6. Spectacle correction (if applicable) for measurement of enrollment visual acuity must

meet the following criteria and be based on a cycloplegic refraction within 6 months:

• Requirements for spectacle correction:
• For patients meeting criteria for only strabismus
• Hypermetropia if corrected must not be undercorrected by more than +1.50 D spherical equivalent, and the reduction in plus sphere must be symmetric in the two eyes. Otherwise, spectacle correction is at investigator discretion.
• For patients meeting criteria for anisometropia or combined-mechanism
• Spherical equivalent must be within 0.50 D of fully correcting the anisometropia
• Hypermetropia must not be undercorrected by more than +1.50 D spherical equivalent, and reduction in plus must be symmetric in the two eyes
• Cylinder power in both eyes must be within 0.50 D of fully correcting the astigmatism
• Cylinder axis in the spectacle lenses in both eyes must be within 6 degrees of the axis of the cycloplegic refraction

Spectacles meeting above criteria must be worn either:

• for 4 weeks immediately prior to enrollment, or
• until visual acuity in amblyopic eye is stable (defined as two consecutive visual acuity measurements at least 4 weeks apart with no improvement of one line or more)
• An acuity measurement done any of the following ways may be considered the first

of two consecutive measurements:

• in current glasses,
• in trial frames with full correction of hypermetropia with cycloplegia, or
• in new glasses.

7. Wearing optimal spectacle correction for a minimum of 4 weeks at the time of enrollment.

8. Ocular examination within 6 months prior to enrollment.

9. Gestational age > 34 weeks and birth weight > 1500 grams

10. Parent willing to accept randomization

11. Parent willing to be contacted and has access to phone

12. Parent does not anticipate relocation outside area within study period.

Exclusion Criteria:

1. Amblyopic eye has myopia worse than -3.00 D spherical equivalent.

2. Prior intraocular or refractive surgery

3. Ocular pathologies that impact vision

4. Cognitive impairment that prohibits accurate data collection

Related Conditions & MeSH terms

• Amblyopia

Intervention

Device:
• IO-therapy Glasses

Locations

Country	Name	City	State
United States	Salus University	Elkins Park	Pennsylvania

Sponsors (1)

Lead Sponsor	Collaborator
Salus University

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Visual Acuity Improvement	visual acuity difference between the primary outcome measure and baseline in the amblyopic eye; visual acuity was measured with ATS- HOTV method	4 weeks for the Intense Group and 12 weeks for the Standard Group
Secondary	Stereoacuity Test	Stereoacuity in arcsec was converted to log scale. so log10(stereo) will be reported.; The higher value indicates a poorer binocular visual function.	4 weeks for the Intense Group and 12 weeks for the Standard Group
Secondary	Objective Total Treatment Hours	Objective total treatment hours at the primary outcome visit measured with a microsensor	4 weeks for the Intense Group and 12 weeks for the Standard Group
Secondary	Objective Adherence	objective adherence measured with a microsensor to the treatment regimen	4 weeks for the Intense Group and 12 weeks for the Standard Group