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Clinical Trials/NCT06600932
NCT06600932
Not yet recruiting
Not Applicable

Effects of Transcranial Magnetic Stimulation on Visual Outcome in Patients After Cataract Surgery

Shanghai High Myopia Study Group1 site in 1 country200 target enrollmentOctober 2024

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Cataract Surgery Experience
Sponsor
Shanghai High Myopia Study Group
Enrollment
200
Locations
1
Primary Endpoint
Visual acuity
Status
Not yet recruiting
Last Updated
last year

Overview

Brief Summary

The goal of this clinical trial is to learn if transcranial magnetic stimulation (TMS) can improve the visual outcomes in patients after cataract surgery. The main question it aims to answer is:

• Does TMS improve the visual outcome in patients after cataract surgery? Researchers will compare TMS to the sham-controlled treatment (exposure to recorded sounds of pulses without real magnetic stimulation) to see if TMS works to improve the visual outcomes of patients after cataract surgery.

Participants will

  • Undergo TMS treatment or a sham-controlled treatment for consecutive 5 days.
  • Visit the clinic once every 2 weeks for checkups and tests.
Registry
clinicaltrials.gov
Start Date
October 2024
End Date
October 2026
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Shanghai High Myopia Study Group
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Post cataract surgery
  • 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 significant opacity of refractive media that affects observation of visual function;
  • History of epileptic seizures;
  • Long term use of psychotropic drugs;
  • Metal implants in the body.

Outcomes

Primary Outcomes

Visual acuity

Time Frame: From enrollment to the end of treatment at 2 weeks

Secondary Outcomes

  • Visual field(From enrollment to the end of treatment at 2 weeks)

Study Sites (1)

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