Clinical Trials Directory

Trials / Completed

CompletedNCT05104138

Eplerenone Versus PDT: Comparative Study by OCTA

OCTA in Central Serous Chorioratinopathy Treated With Oral Eplerenone or Hal-fluence Photodynamic Therapy: a Comparative Study

Status
Completed
Phase
Study type
Observational
Enrollment
30 (actual)
Sponsor
Federico II University · Academic / Other
Sex
All
Age
30 Years – 60 Years
Healthy volunteers

Summary

The study aims to analyze the changes in OCTA parameters and in choroidal thickness in patients affected by central serous chorioretinopathy treated by oral eplerenone and half-fluence photodynamic therapy.

Detailed description

Central serous chorioretinopathy (CSC) is a chorioretinal disease characterized by serous detachment due to the dilatation and hyperpermeability of choroidal vessels resulting in the accumulation of serous fluid between the neurosensory retina and the retinal pigment epithelium. Several studies reported the efficacy of half-fluence photodynamic therapy (PDT) and oral eplerenone in the CSC treatment inducing a reduction of the choroidal hyperpermeability and remodeling the choroidal vascularization. This retrospective study aims to perform a quantitative analysis of retinal and CC vessel density by OCTA at baseline, 3 and 6 months in patients underwent PDT and patients underwent eplerenone.

Conditions

Interventions

TypeNameDescription
DRUGEplerenoneThe patients underwent eplerenone treatment for 6 months
DEVICEThe patients underwent half fluence photodynamic therapy for 6 monthsHalf fluence photodynamic therapy for 6 months

Timeline

Start date
2015-10-01
Primary completion
2017-10-30
Completion
2017-11-30
First posted
2021-11-02
Last updated
2021-11-02

Source: ClinicalTrials.gov record NCT05104138. Inclusion in this directory is not an endorsement.