Clinical Trials Directory

Trials / Recruiting

RecruitingNCT05589974

Choroidal Blood Flow in Acute and Chronic Central Serous Chorioretinopathy

Status
Recruiting
Phase
Study type
Observational
Enrollment
50 (estimated)
Sponsor
Helse Stavanger HF · Other Government
Sex
All
Age
18 Years – 70 Years
Healthy volunteers
Not accepted

Summary

Patients with central serous chorioretinopathy (CSC) will be monitored with laser speckle flow graphy (LSFG), swept source optical coherence tomography (SS-OCT) and SS-OCT angiography (SS-OCTA). The aim is to unveil the flow and pulse wave characteristics of the choroidal circulation in acute CSC and chronic CSC.

Detailed description

Acute CSC - The proposed study tests the hypothesis that choroidal blood flow characteristics are related to the eventual resolution of subretinal fluid. Such relation can shed light on pathophysiological disease mechanisms and constitute a biomarker for disease activity. Chronic CSC - The proposed study tests the hypothesis that choroidal blood flow characteristics will change in response to standard treatment with PDT. The research of such changes will increase the understanding of the treatment response. This knowledge will help in the effort to understand the why some patients are non-responsive to the treatment.

Conditions

Interventions

TypeNameDescription
DRUGVerteporfinChronic CSC are receiving one treatment before the observation period.

Timeline

Start date
2022-10-01
Primary completion
2025-12-31
Completion
2026-07-31
First posted
2022-10-21
Last updated
2024-03-18

Locations

1 site across 1 country: Norway

Source: ClinicalTrials.gov record NCT05589974. Inclusion in this directory is not an endorsement.