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P200TE vs Spectral OCT/SLO Imaging for Retinal Disease

N/A
Waitlist Available
Research Sponsored by Optos, PLC
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Subjects diagnosed with ocular disease including but not limited to: Macular Degeneration, Diabetic Macular Edema, Diabetic Retinopathy, Central Serous Retinopathy, Macular Hole, Epiretinal Membrane, Macular Edema, Glaucoma, and others in the retinal disease study eye(s) as confirmed at the study visit or within the past six (6) months.
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up completion of the study, up to 5 years
Awards & highlights

Study Summary

This trial will compare the performance of a new OCT device to the current standard.

Who is the study for?
This trial is for adults over 18 with vision no worse than 20/400 due to various retinal diseases, including macular degeneration and glaucoma. Participants must be able to understand and sign a consent form, follow instructions, and attend scheduled exams. Those who can't tolerate eye imaging or have unclear ocular media, leukemia, dementia, or multiple sclerosis cannot join.Check my eligibility
What is being tested?
The study compares two devices: the new Optos P200TE and the existing Spectral OCT/SLO in scanning eyes affected by retinal disease. It aims to evaluate which device performs better in capturing detailed images of the retina's condition.See study design
What are the potential side effects?
Since this trial involves non-invasive imaging techniques rather than medication or surgery, side effects are minimal but may include discomfort from bright lights during scanning or temporary visual disturbances after the procedure.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
Select...
I have been diagnosed with an eye disease like Macular Degeneration or Glaucoma.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~completion of the study, up to 5 years
This trial's timeline: 3 weeks for screening, Varies for treatment, and completion of the study, up to 5 years for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Cup/Disc Ratio
Optic Nerve Head Topography
Retinal Nerve Fibre Layer Thickness
+1 more

Trial Design

1Treatment groups
Experimental Treatment
Group I: All patientsExperimental Treatment2 Interventions
All patients will be imaged on the P200TE and Spectral OCT/SLO devices.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
P200TE
2019
N/A
~370

Find a Location

Who is running the clinical trial?

Optos, PLCLead Sponsor
17 Previous Clinical Trials
3,495 Total Patients Enrolled
6 Trials studying Glaucoma
483 Patients Enrolled for Glaucoma
Optos, Inc.UNKNOWN

Media Library

All patients Clinical Trial Eligibility Overview. Trial Name: NCT02921568 — N/A
Glaucoma Research Study Groups: All patients
Glaucoma Clinical Trial 2023: All patients Highlights & Side Effects. Trial Name: NCT02921568 — N/A
All patients 2023 Treatment Timeline for Medical Study. Trial Name: NCT02921568 — N/A

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

Are there any openings for participants in this clinical experiment?

"As per the clinicaltrials.gov database, this particular medical study is no longer open to recruitment. It was first posted on September 1st 2016 and its most recent update was on March 13th 2017. However, there are 298 other trials presently recruiting patients for participation in their respective studies."

Answered by AI
~2 spots leftby Apr 2025