Healthy
Conditions
Keywords
retinal imaging, optical imaging, optical coherence tomography, polarization sensitive coherence tomography
Brief summary
The aim of this pilot study is to assess the ability of a new polarization sensitive optical coherence tomography system to obtain high-quality images of retinal birefringence.
Detailed description
Glaucoma is the second leading cause of blindness in the world. The current clinical standard-of-care procedure to diagnose glaucoma is visual field testing with disc photography. Visual field testing is subjective both in the patient's feedback and the physician's interpretation of this feedback, and disc photography requires a physician's subjective interpretation. As a result, it is estimated that current methods can diagnose glaucoma only after 40% of the nerve fiber layer (NFL) has been lost. Since glaucoma leads to significant changes in both NFL thickness and NFL optical birefringence, non-invasive imaging of these properties could potentially enable diagnosis of glaucoma prior to changes in vision. Optical Coherence Tomography (OCT) is routinely used in retinal imaging, and its ability to detect changes in NFL health is being actively studied. To detect NFL optical birefringence, a specialized variation of OCT termed polarization sensitive OCT (PS-OCT) is required. Because of high noise in PS-OCT images, prior studies have been unable to detect NFL changes in birefringence. We have recently developed new methods for performing highly sensitive polarization-sensitive OCT. These changes are algorithmic in nature, and use the same optical wavelengths and powers as clinically deployed OCT retinal imaging instruments. In benchtop studies, these algorithmic changes improve the signal-to-noise ratio (SNR) of PS-OCT images. We propose to conduct a pilot study in normal, healthy subjects to evaluate if these changes improve the SNR of NFL birefringence images.
Interventions
DEVICEPolarization-Sensitive OFDI
OCT Imaging of the eye
Sponsors
Massachusetts Eye and Ear Infirmary
Massachusetts General Hospital
Study design
Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DEVICE_FEASIBILITY
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
Yes
Inclusion criteria
1. Male or female subjects between the ages of 18-85 years 2. Healthy normal subjects with no significant eye disease, except for mild cataracts 3. Subjects with clear enough cornea or clear enough media to permit imaging 4. Subjects with refractive error between -5.00 sph to +5.00 sph
Exclusion criteria
1. Subjects who have occludable narrow angles (without a patent peripheral iridotomy) or any other ocular or systemic pathology, which precludes safe dilation 2. Subjects whose eyes have been dilated for over 6 hours will not be eligible for imaging. 3. Subjects who do not or cannot understand the instructions for the PS-OCT imaging 4. Subjects who are pregnant and/or breastfeeding. Date of last menstrual cycle will also be included.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Average nerve fiber layer (NFL) birefringence | At time of imaging | Measured birefringence values will be compared to normative values from literature |
Countries
United States
Contacts
Primary ContactBenjamin Vakoc, PhD
Outcome results
None listed