Combined Patching-Atropine for Residual Amblyopia

Amblyopia Clinical Trial

— ATS11  

Official title:

A Randomized Trial to Evaluate Combined Patching-Atropine for Residual Amblyopia

Clinical Trial Details — Status: Terminated

Administrative data

• NCT number: NCT00506675
• Other study ID #: NEI-135
• Secondary ID: 2U10EY011751
• Status: Terminated
• Phase: Phase 3
• First received: July 20, 2007
• Last updated: May 16, 2012
• Start date: October 2007
• Est. completion date: September 2009

Study information

• Verified date: May 2012
• Source: Jaeb Center for Health Research
• Contact: n/a
• Is FDA regulated: No
• Health authority: United States: Federal GovernmentUnited States: Food and Drug Administration
• Study type: Interventional

Clinical Trial Summary

This study is designed to evaluate the effectiveness of treatment of residual amblyopia in children ages 3 to < 10 years with visual acuity of 20/32 to 20/63 in the amblyopic eye. The study is a randomized clinical trial comparing intensive treatment (42 hours per week of patching plus daily atropine) with a control group that will have rapid weaning of existing treatment followed by spectacle correction only (if needed). The primary objective is to determine if this intensive treatment will improve visual acuity in patients with residual amblyopia.

The primary outcome assessment is amblyopic eye visual acuity at 10 weeks.

The primary analytic approach for the amblyopic eye acuity will be a treatment group comparison of the proportion of patients with at least two lines of visual acuity improvement.

Description:

Amblyopia is the most common cause of monocular visual impairment in both children and young and middle-aged adults. Both patching and atropine are accepted treatment modalities for the management of moderate amblyopia in children. Despite best efforts with conventional treatment, some patients fail to achieve normal visual acuity in the amblyopic eye. In a randomized trial conducted by PEDIG comparing atropine versus patching in 3 to 6 year olds with moderate amblyopia (ATS1), 261 of 402 patients (65%) had amblyopic eye visual acuity of 20/32 or worse after 6 months of treatment with patching or atropine. Beyond 6 months, treatment was at investigator discretion, and two years after randomization, 181 of 363 children (50%) still had amblyopic eye visual acuity of 20/32 or worse. In a randomized trial conducted by PEDIG comparing patching regimens, 129 of 181 patients with moderate amblyopia (71%) and 145 of 157 patients with severe amblyopia (92%) had amblyopic eye visual acuity of 20/32 or worse after 4 months of occlusion therapy. Many patients receive treatment beyond 6 months but still fail to achieve normal visual acuity in the amblyopic eye. It is unknown whether an intensive "final push" of combined treatment with daily patching and atropine will improve visual acuity in these patients. Although some clinicians prescribe simultaneous patching and atropine for selected patients, there are no published reports of its effectiveness. Also, we are not aware of reports of response to treatment of residual amblyopia.

The study has been designed as a simple trial that, other than the type of amblyopia therapy being determined through the randomization process, approximates standard clinical practice. Patients will be randomized to one of two treatment regimens:

• Intensive treatment: 42 hours per week of patching combined with daily atropine (1%)

• Control group: Weaning of the current treatment (two hours of daily patching for patients currently using patching and once weekly atropine for patients currently using atropine) for 4 weeks, then no treatment other than spectacles (if needed).

Recruitment information / eligibility

• Status: Terminated
• Enrollment: 55
• Est. completion date: September 2009
• Est. primary completion date: April 2009
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 3 Years to 9 Years

Eligibility

Inclusion Criteria:

• Age 3 to < 10 years

• Amblyopia associated with strabismus, anisometropia, or both

• Visual acuity in the amblyopic eye between 20/32 and 20/63 inclusive

• Visual acuity in the sound eye 20/32 or better and inter-eye acuity difference >= 2 logMAR lines

• Current/previous treatment with patching and/or atropine subject to the following stipulations:

• No simultaneous treatment with patching and atropine in the past 6 months

• No prior use of atropine in combination with the sound eye spectacle lens reduced by more than 1.50 D

• Maximum level of any previous treatment:

• Patching: up to 42 hours per week (averaging 6 hours daily)

• Atropine: up to once daily

• Current treatment with 42 hours per week patching or daily atropine

• No improvement in best-corrected amblyopic eye visual acuity between two consecutive visits at least 6 weeks apart using the same testing method and optimal spectacle correction (if needed), with no improvement defined as follows:

• No lines of improvement

• For patients tested using E-ETDRS, letter score that is no more than 4 letters improved

• Wearing spectacles with optimal correction (if applicable)

• Investigator ready to wean or stop treatment

Exclusion Criteria:

• Current vision therapy or orthoptics

• Ocular cause for reduced visual acuity

• Prior intraocular or refractive surgery

• Strabismus surgery planned within 10 weeks

• Known allergy to atropine or other cycloplegic drugs

• Known skin reactions to patch or bandage adhesives

• Down Syndrome present

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

• Amblyopia

Intervention

Device:
• Patching
42 hours per week of patching

Drug:
• Atropine
daily atropine (1%)

Device:
• Patching
two hours of daily patching for 4 weeks, then no treatment

Drug:
• Atropine
once weekly atropine for 4 weeks, then no treatment

Locations

Country	Name	City	State
United States	Duke University Eye Center	Durham	North Carolina

Sponsors (2)

Lead Sponsor	Collaborator
Jaeb Center for Health Research	National Eye Institute (NEI)

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Distribution of Amblyopic Eye Visual Acuity at 10 Weeks	Visual acuity was measured in each eye using the Amblyopia Treatment Study (ATS) visual acuity testing protocol resulting in a Snellen acuity score that can range from 20/16 to 20/800 for ages 3 to <7; or with the electronic early treatment diabetic retinopathy study (E-ETDRS) method for 7 to <10 year olds which resulted in a letter score that could range from 0 to 97 letters, with 0 being the worst and 97 being the best. Scores were converted to log of minimum angle of resolution (logMAR) equivalents for analyses (lower logMAR value is better than higher logMAR).	10 Weeks	No
Primary	Mean (SD) Distribution of Visual Acuity at 10 Weeks	Visual acuity was measured in each eye using the Amblyopia Treatment Study (ATS) visual acuity testing protocol resulting in a Snellen acuity score that can range from 20/16 to 20/800 for ages 3 to <7; or with the electronic early treatment diabetic retinopathy study (E-ETDRS) method for 7 to <10 year olds which resulted in a letter score that could range from 0 to 97 letters, with 0 being the worst and 97 being the best. Scores were converted to log of minimum angle of resolution (logMAR) equivalents for analyses (lower logMAR value is better than higher logMAR).	10 Weeks	No
Primary	Distribution of Amblyopic Eye Visual Acuity Change From Baseline to 10 Weeks	Change in logMAR from baseline to 10 weeks was calculated, with positive difference indicating improvement. Note one logMAR line = 5 letters or one Snellen line equivalent.	baseline to 10 Weeks	No
Primary	Mean (SD) Change in Visual Acuity in the Amblyopic Eye at the 10 Week Primary Outcome Exam	Change in logMAR from baseline to 10 weeks was calculated, with positive difference indicating improvement. Note one logMAR line = 5 letters or one Snellen line equivalent.	baseline to 10 Weeks	No