Clinical Trials Directory

Trials / Unknown

UnknownNCT02550964

Incidence and Risk Factor of Hydroxychloroquine and Chloroquine Retinopathy

Incidence and Risk Factor Evaluation for Toxic Maculopathy Associated With Hydroxychloroquine and Chloroquine

Status
Unknown
Phase
Study type
Observational
Enrollment
124 (estimated)
Sponsor
Asan Medical Center · Academic / Other
Sex
All
Age
19 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to evaluate the incidence and risk factor of toxic maculopathy who treated with hydroxychloroquine or chloroquine due to their autoimmune disease such as rheumatoid arthritis or systemic lupus erythematosus. Total 5-year of the study periods, the investigators will screen these patients by baseline examination (Fundus photography, fundus autofluorescence, spectral-domain optical coherence tomography, Humphrey visual field test and multifocal electroretinography) and observe with same examination for every year.

Conditions

Interventions

TypeNameDescription
PROCEDUREComposite ExaminationFirst, patients will get the baseline ophthalmologic exam and medical evaluation by physicians. As a diagnostic method, the composite examination including fundus photography, fundus autofluorescence, spectral-domain optical coherence tomography, Humphrey visual field test and multifocal electroretinography will be tested once every year.

Timeline

Start date
2014-01-01
Primary completion
2019-01-01
Completion
2019-01-01
First posted
2015-09-16
Last updated
2015-09-18

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT02550964. Inclusion in this directory is not an endorsement.