Flare Photometry in Uveitis Patients
- Conditions
- Uveitis
- Registration Number
- NCT01897935
- Lead Sponsor
- ChromoLogic, LLC
- Brief Summary
This is a cross sectional study of a novel non-invasive optical flare photometer (OFAM). Patients meeting the inclusion/exclusion criteria will receive a standard eye examination including a slit lamp examination to collect ocular flare data. In addition to the standard eye examination, subjects will receive flare measurements using the OFAM device.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 100
- Age greater than 18 years
- Ability to understand and willingness to sign a written informed consent document.
- To be eligible for the uveitis arm of the study subjects must have active anterior chamber uveitis in one or both eyes as determined by a physician
- To be eligible for the non-inflammatory arm of the study the study subjects must have no ocular inflammation in either eye as determined by a physician.
- Inability to give informed consent
- Exclusion criteria for the uveitis arm: no active disease
- Exclusion criteria for the non-inflammatory arm: Signs of uveitis
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Establish OFAM algorithms for quantitation of ocular flare 3 months OFAM algorithms for quantitation of ocular flare will be established by comparing the output of the OFAM device to the flare measurements obtained during the standard slit lamp examination.
- Secondary Outcome Measures
Name Time Method Determine the impact that various potential confounders such as age and sex have on OFAM Measurements 3 months OFAM data for various sub-groups (age and sex) will be compared in order to evaluate the degree to which each sub-group acts as a confounder for OFAM measurements.
Trial Locations
- Locations (1)
UW Medicine Eye Institute
🇺🇸Seattle, Washington, United States