Actively Recruiting
Central Serous Chorioretinopathy and Micropulse Laser Treatment
Led by Fondazione Policlinico Universitario Agostino Gemelli IRCCS · Updated on 2025-09-23
36
Participants Needed
1
Research Sites
208 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
To evaluate choroidal and choriocapillaris changes in patients with central serous chorioretinopathy, undergone sub threshold micropulse laser treatment, following any improvement with conservative therapy with Acetazolamide and/or Eplerenone
CONDITIONS
Official Title
Central Serous Chorioretinopathy and Micropulse Laser Treatment
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Diagnosis of central serous chorioretinopathy (CSC) with no response to conservative therapy, consisted in Acetazolamide and Eplerenone after six months.
- Foveal serous retinal detachment for at least 6 months.
- Minimum age of 18 years old at the screening time
- Reading and comprehension skills of informed consent
You will not qualify if you...
- Previous retinal treatment for CSC, except for Acetazolamide and Eplerenone
- No diffuse retinal epitheliopathy
- Other concomitant ocular diseases, such as age related macular degeneration, diabetic retinopathy, choroidal neovascularization
- Not controlled glaucoma with eyedrops, or advanced glaucoma
- Myopia or hypermetropia greater than 6 diopters
- Opacities of dioptric media
- Low quality of optical coherence tomography (OCT) and OCT-Angiography scans
- Low quality images of Fluorescein angiography and indocyanine green angiography
- No written consensus signed.
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Fondazione Policlinico Agostino Gemelli, IRCCS
Roma, R, Italy, 00168
Actively Recruiting
Research Team
M
Maria Cristina Savastano, MD, PhD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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