Navigated Microsecond Laser for Chronic Central Serous Chorioretinopathy: MICROPULSE (MICROPULSE)
Central Serous Chorioretinopathy
About this trial
This is an interventional treatment trial for Central Serous Chorioretinopathy focused on measuring retina, photodynamic therapy, micropulse laser, central serous chorioretinopathy
Eligibility Criteria
Inclusion Criteria: 18 years and older vision complaints for more than 6 weeks subretinal fluid confirmed on OCT diagnosis of CSCR confirmed by fluorescein and indocyanine green angiography Signed informed consent Affiliated or beneficiary of health insurance Exclusion Criteria: History of treatment of CSC with other modalities (PDT, eplerenone) in the past 3 months Other macular conditions : Age-related Macular Degeneration (AMD), polypoidal vasculopathy, choroidal neovascularization Cataract or opacities interfering with acquisition or treatment Myopia> 6 diopter Visual acuity<20/200 Treatment with steroids (per-os, inhaled or cutaneous) in the past 3 months Intra-vitreal injections of anti-VEGF (Vascular Endothelial Growth Factor) or steroids in the past 3 months History of allergy to fluorescein or indocyanine Inability to agree to participate to the study Pregnant or breastfeeding woman Patient under legal protection
Sites / Locations
Arms of the Study
Arm 1
Experimental
micropulse laser
treatment with confluent spots over the area of focal leak on the earliest phase of fundus fluorescein angiography on Navilas® system using 5% duty cycle with 100 micron spot size with 200 ms envelope. Thirty percent of threshold laser burn power was used.