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
| Type | Name | Description |
|---|---|---|
| DRUG | Eplerenone | The patients underwent eplerenone treatment for 6 months |
| DEVICE | The patients underwent half fluence photodynamic therapy for 6 months | Half 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.