Central Serous Chorioretinopathy and Micropulse Laser Treatment
Recruiting now
Conditions studied: Central Serous Chorioretinopathy
In brief
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
Key facts
- Study ID
- NCT06346405
- Run by
- Fondazione Policlinico Universitario Agostino Gemelli IRCCS
- People needed
- 36
- Starts
- 2023-05-31
- Expected to finish
- 2027-05-31
- Last updated by the study team
- 2025-09-23
Who can join
Age: 18 and older, up to 70. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- 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 may not qualify if…
- 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.
Where it is running
- Fondazione Policlinico Agostino Gemelli, IRCCS — Roma, R, Italy (enrolling)
Full record on ClinicalTrials.gov
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