Central Serous Chorioretinopathy and Micropulse Laser Treatment

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-70
SponsorFondazione Policlinico Universitario Agostino Gemelli IRCCS

About this trial

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

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

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

Disqualifiers

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

Trial population

Patients older than 18 years old, with diagnosis of central serous chorioretinopathy since at least 6 months, undergone Acetazolamide and/or Eplerenone therapy with no improvement after 6 months.

Trial design

Design model

Case-only

Time perspective

Prospective

Treatments tested in this trial

  • Subthreshold Micropulse Laser Treatment

    Other intervention

    Subthreshold micropulse laser treatment consists in 33 spots of 100 microns, distance among each spot of 2.50 microns, duration of 200 sec, power of 250 milliwatt (mW) duty cycle 5%.

Treatment groups

No treatment groups listed

Trial outcomes

Primary outcomes

1

Vessel density changes

Evaluation of changes in vessel density of choriocapillaris by optical coherence tomography (OCT) angiography before and after treatment

Time frame
12 and 24 months

Secondary outcomes

1

Choroidal thickness

Evaluation of changes in choroidal thickness before and after treatment.

Time frame
12 and 24 months
2

Choroidal thickness and vessel density

Correlation among changes in choroidal thickness and changes in vessel density of choriocapillary with best corrected visual acuity.

Time frame
12 and 24 months
3

Qualitative analysis of retino-choroidal vascularization with identification of vascular pattern

To qualitatively evaluate the vascular patterns using optical coherence tomography (OCT) - angiography and to verify if a particular one is associated with a greater response to subthreshold micropulse laser treatment.

Time frame
12 and 24 months
4

Metamorphopsia

Evaluation of quantitative improvement of metamorphosia by M-CHARTS after treatment.

Time frame
12 and 24 months

Other outcomes

Sponsors and contacts

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