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NCT02277119 · ClinicalTrials.gov registry record · NA
Clinical Study of the Optic Disc Parameters
A NA study, sponsored by Topcon Medical Systems.
- Completed
- Registry status
- NA
- Development phase
- 109
- Enrollment target
NCT02277119: Completed NA study, sponsored by Topcon Medical Systems.
NCT02277119 is a NA study that has completed, run by Topcon Medical Systems. The registered enrollment target is 109 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (92% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02277119, a NA study, has completed, sponsored by Topcon Medical Systems.
- COMPLETED
- Registry status
- NA
- Development phase
- 109 participants
- Enrollment target
Study Summary
Assess the repeatability and agreement of the Optic Disc Parameters, Retinal Nerve Fiber Layer (RNFL) Thickness, and Full Retinal Thickness between the Maestro and iVue OCT devices
Primary Outcome
Reporting of the Optic Disc Size difference between the Maestro and iVue
Interventions
- DEVICE iVue
- DEVICE Maestro
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 109 participants |
| Start Date | 2014-10 |
| Est. Completion | 2015-02 |
| Phase | NA |
What the finished NCT02277119 record still lists
NCT02277119 is an interventional study that assigns participants to a tested intervention. The registered 109 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (92% lower).
The record links to 0 conditions, and to 2 interventions - of which iVue is the first listed.
NCT02277119 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT02277119 about?
NCT02277119 is a clinical study titled "Clinical Study of the Optic Disc Parameters". Assess the repeatability and agreement of the Optic Disc Parameters, Retinal Nerve Fiber Layer (RNFL) Thickness, and Full Retinal Thickness between the Maestro and iVue OCT devices
What is the current status of trial NCT02277119?
This trial is currently completed. It is a NA study. The enrollment target is 109 participants. The study started on 2014-10. Estimated completion is 2015-02.
What interventions are being tested in trial NCT02277119?
The interventions under investigation include: iVue (DEVICE), Maestro (DEVICE).
Who is sponsoring clinical trial NCT02277119?
This trial is sponsored by Topcon Medical Systems, which has 24 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT02277119's enrollment target sits among peer trials
109 825th of 2000 higher than 1,176 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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