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Imaging of Vitreous Opacities in a Canadian Population

Not Applicable
Recruiting
Conditions
Floaters
Vitreous Opacities
Interventions
Device: SVO-ID
Registration Number
NCT06204848
Lead Sponsor
PulseMedica
Brief Summary

The goal of this clinical trial is to capture imaging data of eye floaters in the population to build an imaging database to learn more about them in. Participants will imaged with an investigational ophthalmic imaging device to capture images of their floaters.

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
125
Inclusion Criteria
  • Aged 18 years or older
  • Symptomatic vitreous opacities (floaters) in vision
  • Clear ocular media, to allow a clear view of the vitreous for the SVO-ID
Exclusion Criteria
  • Younger than 18 years of age
  • Presence of vitreous hemorrhage
  • Cataract Grade 3 and above
  • Opacification of lens, cornea, or vitreous
  • Diagnosis of narrow angle glaucoma
  • Refractive error is outside the range of -6D to+3D
  • Astigmatism is outside the range of +/-2D of cylinder

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Imaging using the SVO-IDSVO-IDPatients will have their eyes imaged with the SVO-ID as part of a study visit.
Primary Outcome Measures
NameTimeMethod
Successful capture of SLO and OCT imaging data of SVOs for algorithm developmentThrough study completion, an average of 6-8 months

Successful collection of SLO and OCT imaging data

Secondary Outcome Measures
NameTimeMethod
Collection of patient-reported symptomsThrough study completion, an average of 6-8 months

Patient feedback regarding symptoms related to SVOs being imaged

Trial Locations

Locations (1)

Alberta Retina Consultants

🇨🇦

Edmonton, Alberta, Canada

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