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Amblyopia is the leading cause of monocular visual impairment in children and adults. Despite conventional treatment with patching or eye drops, many older children and adults do not achieve normal vision in the amblyopic eye.
Donepezil is an acetylcholinesterase inhibitor that increases levels of the neurotransmitter acetylcholine in the brain. Use of acetylcholinesterase inhibitors has been demonstrated by the Hensch lab (Department of Neurology, FM Kirby Neurobiology Center) at Boston Children's Hospital to improve vision and reverse amblyopia in animal models.
The purpose of this study is to evaluate the efficacy of oral donepezil as treatment for residual amblyopia (20/50 - 20/400) in patients 8 years of age and older.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Donepezil | Experimental |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Donepezil | Drug | Oral Donepezil Daily Initial Dosage: Donepezil 5 mg tablets will be used. 1/2 tablet (≈2.5 mg)/day for 8 to 17 year olds OR 1 tablet (5 mg)/day for ≥18 year olds. Dosage Escalation: Donepezil may be increased by 1/2 tablet (≈2.5 mg)/day every 4 weeks if the amblyopic eye visual acuity has not improved by ≥5 letters or 1 logMAR line to a maximum dosage of 1 1/2 tablets (≈7.5 mg)/day for 8 to 17 year olds OR 2 tablets (10 mg)/day for ≥18 year olds. |
| Measure | Description | Time Frame |
|---|---|---|
| Amblyopia Eye Visual Acuity Improvement | Study treatment will last for 12 weeks. Primary outcome measure is analysis of the proportion of subjects with improvement in amblyopic eye visual acuity of ≥ 15 letters or 3 logMAR lines at 22 weeks after 10 weeks off study treatment. | 22 weeks after enrollment |
| Measure | Description | Time Frame |
|---|---|---|
| Amblyopic Eye Visual Acuity | Analysis of amblyopia eye visual acuity measured at each visit. | 4, 8, 12, and 22 weeks after enrollment |
| Recurrence of Amblyopia after 10 Weeks Off Study Treatment |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Carolyn Wu, MD | Boston Children's Hospital | Principal Investigator |
| David G. Hunter, MD, PhD | Boston Children's Hospital | Principal Investigator |
| Bharti Gangwani, MD | Boston Children's Hospital | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Boston Children's Hospital | Boston | Massachusetts | 02115 | United States | ||
| Boston Children's Hospital at Waltham |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 21071629 | Background | Morishita H, Miwa JM, Heintz N, Hensch TK. Lynx1, a cholinergic brake, limits plasticity in adult visual cortex. Science. 2010 Nov 26;330(6008):1238-40. doi: 10.1126/science.1195320. Epub 2010 Nov 11. |
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| ID | Term |
|---|---|
| D000550 | Amblyopia |
| ID | Term |
|---|---|
| D001927 | Brain Diseases |
| D002493 | Central Nervous System Diseases |
| D009422 | Nervous System Diseases |
| D014786 | Vision Disorders |
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| ID | Term |
|---|---|
| D000077265 | Donepezil |
| ID | Term |
|---|---|
| D007189 | Indans |
| D007192 | Indenes |
| D011084 | Polycyclic Aromatic Hydrocarbons |
| D006841 | Hydrocarbons, Aromatic |
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|
|
| Patching | Other | Patching: 2 hours of daily patching will also be prescribed for 8 to 17 year olds only. |
|
Study treatment will be discontinued after 12 weeks. Amblyopic eye visual acuity at 12 weeks and 22 weeks will be compared. Analysis of the proportion of subjects with recurrence of amblyopia after 10 weeks off study treatment.
| 22 weeks after enrollment |
| Adverse Events | Analysis of the proportion of subjects reporting adverse events. | 4, 8, 12, and 22 weeks after enrollment |
| Adverse Events Requiring Discontinuation of Study Treatment | Analysis of the proportion of subjects requiring discontinuation of study treatment secondary to adverse events. | 4, 8, and 12 weeks after enrollment |
| Completion of Study Treatment | Analysis of the proportion of subjects completing study treatment. | 12 weeks after enrollment |
| Sound Eye Visual Acuity | Analysis of sound eye visual acuity at 22 weeks to assess any adverse effect on the occluded eye. | 22 weeks after enrollment |
| Waltham |
| Massachusetts |
| 02453 |
| United States |
| Boston Children's Physicians South | Weymouth | Massachusetts | 02190 | United States |
| D012678 | Sensation Disorders |
| D009461 | Neurologic Manifestations |
| D005128 | Eye Diseases |
| D012816 | Signs and Symptoms |
| D013568 | Pathological Conditions, Signs and Symptoms |
| D006844 |
| Hydrocarbons, Cyclic |
| D006838 | Hydrocarbons |
| D009930 | Organic Chemicals |
| D010880 | Piperidines |
| D006573 | Heterocyclic Compounds, 1-Ring |
| D006571 | Heterocyclic Compounds |
| D011083 | Polycyclic Compounds |