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The change of amblyopia in visual function and event-related potential after repetitive transcranial magnetic stimulation (rTMS)

The change of amblyopia in visual function and event-related potential after repetitive transcranial magnetic stimulation (rTMS)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-INR-17011628
Enrollment
Unknown
Registered
2017-06-11
Start date
2017-07-01
Completion date
Unknown
Last updated
2017-06-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Amblyopia

Interventions

Control Group:Pseudo Repetitive Transcranial Magnetic Stimulation

Sponsors

West China Hospital, Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 30 Years

Inclusion criteria

Inclusion criteria: 1. Sixty individuals with amblyopia (aged 18–30 years, 30 males) will take part in the experiment, including anisometropic amblyopia, ametropia amblyopia and strabismic amblyopia (Most of them will have suffered from microstrabism following operation). The subjects and controls will be similar with respect to age, gender and educational level; 2. The visual acuity of the amblyopic eye should be less than LogMAR 0.5.

Exclusion criteria

Exclusion criteria: 1. Pattern of fixation will be evaluated and those with poor fixation will be excluded; 2. history or evidence of intraocular surgery, gross structural abnormalities, retinal disease, optic nerve abnormalities, and a known or suspected neurological condition will be excluded; 3. Any participant with a abnormal color vision was also excluded from the study.

Design outcomes

Primary

MeasureTime frame
Accuracy in Face Discrimination;Reaction Times in Face Discrimination;the significant change of the results of event-related potentials;stereoacuity;disparity-evoked VEP;

Countries

China

Contacts

Public ContactLiu Longqian

Department of Ophthalmology, West China Hospital, Sichuan University

b.q15651@hotmail.com+86 189 8060 1759

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026