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Clinical Trials/NCT05589974
NCT05589974
Recruiting
Not Applicable

Choroidal Blood Flow in Acute and Chronic Central Serous Chorioretinopathy

Helse Stavanger HF1 site in 1 country50 target enrollmentOctober 1, 2022

Overview

Phase
Not Applicable
Intervention
Verteporfin
Conditions
Central Serous Chorioretinopathy
Sponsor
Helse Stavanger HF
Enrollment
50
Locations
1
Primary Endpoint
Change in mean blur rate
Status
Recruiting
Last Updated
2 years ago

Overview

Brief 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.

Registry
clinicaltrials.gov
Start Date
October 1, 2022
End Date
July 31, 2026
Last Updated
2 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Able to sign informed consent
  • Possible to obtain fundus imaging
  • Acute CSC ˂4 months of duration in one eye, defined as:
  • Subfoveal presence of SRF on OCT
  • Present attack is 1st -3rd attack of CSC
  • b) Patient history and examination consistent with acute CSC c) Characteristic appearance of acute CSC on fundus autofluorescence (FAF) and OCT
  • Chronic CSC ≥4 months of duration in one eye, defined as:
  • Subfoveal presence of SRF on OCT
  • Subjective visual loss/symptoms
  • Characteristic appearance of chronic CSC on FAF, fluorescein angiography (FA), and indocyanin angiography (ICGA) and OCT

Exclusion Criteria

  • History of retinal disease other than CSC (e.g. retinal detachment)
  • Contraindications for FA, ICGA or PDT (only for chronic CSC)

Arms & Interventions

Chronic

Patients with chronic CSC, i.e. symptoms and SRF for more than 4 months.

Intervention: Verteporfin

Outcomes

Primary Outcomes

Change in mean blur rate

Time Frame: 6 months

Relative changes in choroidal blood flow

Change in pulse wave form analysis

Time Frame: 6 months

Changes in the shapes of pulse curves

Secondary Outcomes

  • Change in choroidal density(6 months)
  • Change in choroidal thickness(6 months)

Study Sites (1)

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