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Central Serous Chorioretinopathy and Micropulse Laser Treatment (LEVEO)

I

Institute of Hospitalization and Scientific Care (IRCCS)

Status

Enrolling

Conditions

Central Serous Chorioretinopathy

Treatments

Other: Subthreshold Micropulse Laser Treatment

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

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

Enrollment

36 estimated patients

Sex

All

Ages

18 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 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

Exclusion criteria

  • 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.

Trial contacts and locations

1

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Central trial contact

Maria Cristina Savastano, MD, PhD

Data sourced from clinicaltrials.gov

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