Evaluation on Visual Outcome of TMS
Not Applicable
Not yet recruiting
- Conditions
- Visual Impairment
- Interventions
- Procedure: TMSProcedure: Control
- Registration Number
- NCT06612190
- Lead Sponsor
- Evidence Based Cataract Study Group
- Brief Summary
The goal of this clinical trial is to learn if transcranial magnetic stimulation (TMS) can improve the visual outcomes in patients with visual impairment. The main question it aims to answer is:
• Does TMS improve the visual outcome in patients who suffer from visual impairment? Researchers will compare TMS to the control group who will not receive effective TMS treatment) to see if TMS works to improve the visual outcomes of the patients.
Participants will
* Undergo TMS treatment or no effective TMS for consecutive 5 days.
* Visit the clinic once every 2 weeks for checkups and tests.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- NOT_YET_RECRUITING
- Sex
- All
- Target Recruitment
- 300
Inclusion Criteria
- Post cataract surgery or clear lens
- Best-corrected visual acuity less than 0.1logMAR
Exclusion Criteria
- Diagnosed with cognitive impairment or mental disorders and unable to cooperate with treatment;
- Diagnosed with ocular diseases that affect observation of visual function;
- History of epileptic seizures;
- Long term use of psychotropic drugs；
- Metal implants in the body.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description TMS TMS - Control Control -
- Primary Outcome Measures
Name Time Method Visual acuity From enrollment to the end of treatment at 6 months
- Secondary Outcome Measures
Name Time Method Visual field From enrollment to the end of treatment at 6 months
Trial Locations
- Locations (1)
Eye and Ear, Nose Throat Hospital of Fudan University
🇨🇳Shanghai, Shanghai, China