glaucoma
Conditions
Interventions
Experimental group:Conventional treatment plus vision restoration training
Control group:Conventional treatment and perform no effect stimulation
Sponsors
Beijing Shijitan Hospital, Capital Medical University
Eligibility
Sex/Gender
All
Age
6 Years to 70 Years
Inclusion criteria
Inclusion criteria: the patients with stable glaucoma without monocular blindness, and have sufficient experience in Octopus 101 perimeter (Haag-Steit AG, Koeniz-Berne, Switzerland) standard automated perimetry to minimize the learning effect; the damage of ONH and retinal nerve fiber layer defect (RNFLD) were confirmed by both optical coherence tomography and fundus image. The VF tests were classified as reliable if the false positive response rate was <15%, and false-negative responses was <25%.
Exclusion criteria
Exclusion criteria: The exclusion criteria were defined with the history of any other optic neuropathy; any retinal and macular disease; optic media opacities; spherical refractive error greater than ±6 diopters; and an astigmatism greater than +/-3 diopters. Presence of any chronic-degenerative disease of the nervous system, motor disturbance, neglect, nystagmus or other forms of impairments to fixate, amblyopia, photosensitivity, history of trauma, any other ocular disease or ocular surgery at least one year prior to recruitment or expected ocular surgery within the six months after study entry.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| visual field; | — |
Countries
China
Contacts
Public ContactLu Yan
Department of Ophthalmology, Beijing Shijitan Hospital, Capital Medical University
Outcome results
None listed