Recruiting NCT06566339
Robotic OCT for ER Anterior Eye Exams
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Robotically Aligned Eye Imaging System.
- Who it may be relevant to
- Registry conditions: Develop and Test Robotically Assisted Imaging System for the Front of the Eye. Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- United States
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
Robotically Assisted Anterior Eye Examinations for Acute Eye Care
Overview
The purpose of this study is to develop and test a robotically assisted imaging system for the front of the eye with a goal of helping eye care through the emergency department.
Interventions
- Device Robotically Aligned Eye Imaging System
Robotically Aligned Eye Imaging System is a non-contact, micrometer scale imaging technique that provides clinicians and researchers with high resolution in vivo images sufficient to visualize layered microanatomy in 3D. The study team will develop hardware systems and software algorithms necessary for acquiring ocular anterior segment images for those seeking eye care in emergency department settings.
Primary outcome measures
- Sensitivity [Time frame: Day 1]
- Specificity [Time frame: Day 1]
Eligibility criteria
Inclusion criteria
- Adult patients 18 years of age and older
- Presenting with ocular complaints potentially indicative of an anterior segment pathology (e.g., foreign body sensation, red eye, pain)
Exclusion criteria
- Hemodynamically unstable patients (e.g., undergoing active resuscitation efforts)
- Patients with potential penetrating trauma to the eye who may need immediate surgical care
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: Yes
Study design
- Allocation
- Non-randomized
- Model
- Single group
- Masking
- Open label
- Primary purpose
- Diagnostic
Study locations
United States · 1 center
- Duke Eye Center — Durham
Identifiers
NCT: NCT06566339 · Pro00115313