Imaging of Vitreous Opacities in a Canadian Population
Not Applicable
Recruiting
- Conditions
- FloatersVitreous 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
Group Intervention Description Imaging using the SVO-ID SVO-ID Patients will have their eyes imaged with the SVO-ID as part of a study visit.
- Primary Outcome Measures
Name Time Method Successful capture of SLO and OCT imaging data of SVOs for algorithm development Through study completion, an average of 6-8 months Successful collection of SLO and OCT imaging data
- Secondary Outcome Measures
Name Time Method Collection of patient-reported symptoms Through 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