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Dexamethasone implant in the treatment of central serous chorioretinopathy

Not Applicable
Conditions
Health Condition 1: H357- Separation of retinal layers
Registration Number
CTRI/2022/01/039632
Lead Sponsor
Hyderabad Eye Research Foundation
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Open to Recruitment
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1. Patients with non-resolving and recurrent CSCR with focal, multifocal, or diffuse leaks on FA

2. Eyes with focal leaks within 1000microns of the center of fovea in chronic CSCR

3. Best corrected vision score of 73 to 34 at test distance of 4 meters on ETDRS chart at recruitment (Snellen equivalent 20/40 to 20/200)

4. Decrease in vision primarily secondary to CSCR

5. Willing to sign informed consent form

Exclusion Criteria

1. Laser or pharmacological treatment for CSCR in previous six months

2. Eyes with choroidal neovascularization demonstrated on OCTA/FA/ICGA

3. Fellow eye vision worse than 20/200

4. Aphakia

5. Patients with glaucoma.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Complete resolution of SRF as determined on OCT <br/ ><br>The disappearance of intraretinal cystoid spaces <br/ ><br>Visual acuity change <br/ ><br>Change in contrast sensitivity <br/ ><br>Change in mfERG waveforms <br/ ><br>Change in intraocular pressure <br/ ><br>Timepoint: 6 and 12 weeks
Secondary Outcome Measures
NameTimeMethod
Reappearance of disease <br/ ><br>% Requiring retreatment <br/ ><br>Changes in PED height <br/ ><br>Lens changes <br/ ><br>% Requiring medical/surgical treatment for glaucoma <br/ ><br>Timepoint: 3,6,9 and 12 months
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