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The Effect of Light Deprivation on Visual Functions in Adult Amblyopes

Boston Children's Hospital logo

Boston Children's Hospital

Status

Withdrawn

Conditions

Amblyopia
Visual Impairment
Anisometropia

Treatments

Device: Blindfold

Study type

Interventional

Funder types

Other

Identifiers

NCT02799836
P00008306

Details and patient eligibility

About

Amblyopia is a significant health problem, affecting up to 4% of the population in the United States. Amblyopia, commonly known as "lazy eye," is a developmental visual disorder in which one or both eyes suffer from poor vision as a result of being disadvantaged in early life. Strabismus, or eye misalignment, such as crossed eyes (esotropia) or wandering eyes (exotropia), and anisometropia, or a power difference between the eyes, are the most common causes of amblyopia. If conventional treatment, such as patching the better seeing eye, is not initiated during the critical period of visual development, lasting visual impairment may persist throughout life. This critical period of visual development has been thought to end around age 10. However, recent research has demonstrated that the critical period of visual development can be extended into adulthood. Complete light deprivation in animal models has restored plasticity in the visual cortex and has demonstrated drastic recovery of vision in amblyopic eyes. The objective of this pilot study is to evaluate the impact of complete light deprivation on visual function in a cohort of human adults with severe amblyopia from anisometropia.

Sex

All

Ages

18 to 50 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Amblyopia, defined as decreased vision, less than or equal to 20/100, in one eye secondary to anisometropia
  • Age 18-50 years

Exclusion criteria

  • Strabismus
  • Eye pathology, such as cataract, corneal disorder, maculopathy, glaucoma,
  • Mental health diagnosis, such as depression, schizophrenia, bipolar disorder or anxiety disorder

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

0 participants in 1 patient group

Light deprived study subjects
Experimental group
Description:
Study subjects who are blindfolded for 48 hours
Treatment:
Device: Blindfold

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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