Actively Recruiting

Age: 18Years - 70Years
All Genders
NCT05589974

Choroidal Blood Flow in Acute and Chronic Central Serous Chorioretinopathy

Led by Helse Stavanger HF · Updated on 2024-03-18

50

Participants Needed

1

Research Sites

199 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

Choroidal Blood Flow in Acute and Chronic Central Serous Chorioretinopathy

Who Can Participate

Age: 18Years - 70Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Able to sign informed consent
  • Possible to obtain fundus imaging
  • Acute CSC of less than 4 months duration in one eye, defined by subfoveal presence of subretinal fluid on OCT and 1st to 3rd attack
  • Patient history and exam consistent with acute CSC
  • Characteristic acute CSC appearance on fundus autofluorescence and OCT
  • Chronic CSC of 4 months or more duration in one eye, defined by subfoveal presence of subretinal fluid on OCT
  • Subjective visual loss or symptoms
  • Characteristic chronic CSC appearance on fundus autofluorescence, fluorescein angiography, indocyanin angiography, and OCT
  • Patient history and exam consistent with chronic CSC
Not Eligible

You will not qualify if you...

  • History of retinal disease other than CSC such as retinal detachment
  • Contraindications for fluorescein angiography, indocyanin angiography, or photodynamic therapy (for chronic CSC)

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Stavanger University Hospital, Department of Ophthalmology

Stavanger, Norway, 4016

Actively Recruiting

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Research Team

V

Vegard Forsaa, MD PhD

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

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