Clinical Trials Directory

Trials / Completed

CompletedNCT00963131

High-dose Antioxidants for Central Serous Chorioretinopathy

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
60 (estimated)
Sponsor
Prince of Songkla University · Academic / Other
Sex
All
Age
30 Years – 50 Years
Healthy volunteers
Not accepted

Summary

Central serous chorioretinopathy (CSC) is the serous neurosensory detachment that usually involves the macular area. It is common in patients between 30-50 years old and effects male more often than female with the ratio of 5-10. The common risk factors are psychologic stress, type A personality, systemic steroid use, hypertension and pregnancy. The treatment is usually observation especially in the first three-months. The laser or photodynamic therapy should be considered when the condition does not improve after that time. Nevertheless, the pathogenesis of CSC is still not well understood but the study from indocyanine green angiography showed the choroidal vascular hyperpermeability and abnormal leakage. The causes of this abnormality are supposed to be from nitric oxide, prostaglandins or even free oxidative radicals. From this hypothesis, the oxidative process might be involved in the pathogenesis of the disease especially in the early stage. This study is to determine the effect of antioxidants drugs in the acute stage of CSC and to determine whether they can improve the outcomes of the disease.

Conditions

Interventions

TypeNameDescription
DRUGantioxidants tabletsvitamin A 6600 IU, vitamin C 400 mg, vitamin E 150 IU, riboflavin 10 mg, zinc 60 mg, copper 4 mg, selenium 40 mg, manganese 4 mg and lutein/zeaxanthin 4000 micrograms.

Timeline

Start date
2004-12-01
Primary completion
2008-12-01
Completion
2009-06-01
First posted
2009-08-21
Last updated
2009-12-30

Locations

1 site across 1 country: Thailand

Source: ClinicalTrials.gov record NCT00963131. Inclusion in this directory is not an endorsement.