Robot-assisted imaging for eye exams in emergency settings
Robotically Assisted Anterior Eye Examinations for Acute Eye Care
This study is testing a new robot that helps doctors take better pictures of the front of the eye in emergency rooms to improve care for patients with eye problems.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 93 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Duke University Academic / other |
| Locations | 1 site (Durham, North Carolina) |
| Trial ID | NCT06566339 on ClinicalTrials.gov |
What this trial studies
This study aims to develop and test a robotically assisted imaging system designed for examining the front of the eye in emergency department settings. The approach focuses on enhancing the accuracy and efficiency of ocular assessments for patients presenting with various eye-related complaints. By utilizing advanced robotic technology, the study seeks to improve diagnostic capabilities and streamline patient care in urgent situations.
Who should consider this trial
Good fit: Ideal candidates for this study are adult patients aged 18 and older who present with ocular complaints suggestive of anterior segment pathology.
Not a fit: Patients who are hemodynamically unstable or have penetrating eye trauma requiring immediate surgical intervention may not benefit from this study.
Why it matters
Potential benefit: If successful, this technology could significantly enhance the speed and accuracy of eye examinations in emergency departments, leading to better patient outcomes.
How similar studies have performed: While similar robotic imaging technologies have shown promise in other medical fields, this specific application for emergency eye exams is relatively novel and untested.
Eligibility criteria
Show full inclusion / exclusion 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
Where this trial is running
Durham, North Carolina
- Duke Eye Center — Durham, North Carolina, United States (Recruiting)
Study contacts
- Principal investigator: Anthony Kuo, MD — Duke University
- Study coordinator: Terry H. Coordinator
- Email: teresa.hawks@duke.edu
- Phone: 919-681-1569
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.