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Dexamethasone implant in the treatment of central serous chorioretinopathy

Efficacy of intravitreal dexamethasone injection in chronic, atypical, and recurrent central serous chorioretinopathy. A prospective pilot study. - NIL

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/01/039632
Enrollment
10
Registered
2022-01-21
Start date
Unknown
Completion date
Unknown
Last updated
2022-10-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: H357- Separation of retinal layers

Interventions

Intervention1: Intravitreal Ozurdex Implantation: Intravitreal Ozurdex Implantation Single Dose Follow up- Weekly for 2 weeks, 6 weeks, 12 weeks, 3 monthly thereafter till 1 year Control Intervention1

Sponsors

Hyderabad Eye Research Foundation
Lead Sponsor

Eligibility

Inclusion criteria

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

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.

Design outcomes

Secondary

MeasureTime frame
Reappearance of disease % Requiring retreatment Changes in PED height Lens changes % Requiring medical/surgical treatment for glaucoma Timepoint: 3,6,9 and 12 months

Primary

MeasureTime frame
Complete resolution of SRF as determined on OCT The disappearance of intraretinal cystoid spaces Visual acuity change Change in contrast sensitivity Change in mfERG waveforms Change in intraocular pressure Timepoint: 6 and 12 weeks

Countries

India

Contacts

Public ContactMohammed Hasibur Rahman

L V Prasad Eye Institute

umesh@lvpei.org9853011697

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026