AR Training Versus Patching in Unilateral Amblyopia
ConditionAmblyopia Unilateral
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age5-55
SponsorEye & ENT Hospital of Fudan University
About this trial
This is a multi-center, randomized controlled trial to compare the effectiveness of AR training with patching for the treatment of unilateral amblyopia.
Specific Aim 1 (Primary): To compare the improvement of visual acuity in the amblyopic eye between AR training and patching for the treatment of unilateral amblyopia.
Specific Aim 2 (Secondary): To compare the improvement of visual functions between AR training and patching for the treatment of unilateral amblyopia.
Eligibility criteria
Qualifiers
Aged 5-55 years (including 5 years and 55 years);
Best-corrected visual acuity worse than 20/30 but no worse than 20/200 in the amblyopic eye, interocular difference of 2 or more lines, with the better eye within the normal range;
Patients have applied optical refractive correction for more than 3 months;
Ability attend visits and complete the treatment;
Disqualifiers
Organic eye diseases preventing the establishment of good vision (e.g. ptosis, media opacity, nystagmus, paracentral fixation, acute inflammation like keratitis, optic nerve diseases like glaucoma, retinal diseases);
Lesions of the brain preventing the establishment of good vision (e.g. cortical visual impairment);
Implantable electronic device;
A history of ocular surgery (except strabismus surgery) affecting vision (e.g. retinal detachment repair);
Trial design
Treatments tested in this trial
- AR training
- Patching
Treatment groups
114 Participants
are divided into 2 treatment groupsSponsors and collaborators
Eye & ENT Hospital of Fudan University
Lead sponsor
First Affiliated Hospital of Fujian Medical University
Collaborator
Shanghai Tong Ren Hospital
Collaborator
Jiangsu Provincial People's Hospital
Collaborator
Source ClinicalTrials.gov