Skip to main content
Clinical Trials/NCT05705778
NCT05705778
Recruiting
Not Applicable

Prognostic Value of Plasma Biomarkers Among Patients With Amblyopia

Zhongshan Ophthalmic Center, Sun Yat-sen University1 site in 1 country600 target enrollmentNovember 1, 2022
ConditionsAmblyopia

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Amblyopia
Sponsor
Zhongshan Ophthalmic Center, Sun Yat-sen University
Enrollment
600
Locations
1
Primary Endpoint
Plasma protein predictor screening for visual acuity improvement following amblyopia therapy using Tandem Mass Tags proteomics
Status
Recruiting
Last Updated
3 years ago

Overview

Brief Summary

This prospective study aims to observe the predictive effect of peripheral blood plasma biomarker on the outcome of treatment in children with different types of amblyopia. We also investigated the mechanism of neuromodulation in the visual development of amblyopic children.

Registry
clinicaltrials.gov
Start Date
November 1, 2022
End Date
October 31, 2027
Last Updated
3 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Jingrong Li

Professor

Zhongshan Ophthalmic Center, Sun Yat-sen University

Eligibility Criteria

Inclusion Criteria

  • Diagnosed with amblyopia
  • 3-12 years of age
  • Able to tolerate amblyopia treatment
  • Agree to be involved in this study and agree to have a follow up visit every 3 months.

Exclusion Criteria

  • Have previous treatment history before
  • Have pathological ocular anomalies known to cause reduced visual acuity
  • Have previous psychiatric, visual or neurological disorders
  • Have eccentric fixation and/or abnormal retinal correspondence
  • Have attention disorder and learning disability that cannot comprehend psychophysical test instructions given and/or consent for themselves

Outcomes

Primary Outcomes

Plasma protein predictor screening for visual acuity improvement following amblyopia therapy using Tandem Mass Tags proteomics

Time Frame: 2 years after including into this clinical trial

Peripheral blood will be collected prior and after treatment. The plasma will be separated and Tandem Mass Tags will be used for proteomics. We will detect the different expression of plasma protein between successfully treated and untreated amblyopia patients to find biomarkers that predict amblyopia treatment success. Amblyopia treatment success is defined as best corrected visual acuity (BCVA) improvement of 3 or more logMAR lines.

Study Sites (1)

Loading locations...

Similar Trials