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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05726058
Other study ID # HP-00102645
Secondary ID 1R44EY034064-01
Status Recruiting
Phase N/A
First received
Last updated
Start date March 30, 2023
Est. completion date April 30, 2025

Study information

Verified date April 2024
Source University of Maryland, Baltimore
Contact Osamah J Saeedi, MD, MS
Phone (410) 328-5929
Email osaeedi@som.umaryland.edu
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The goal of this clinical trial is to investigate the use of an FDA-cleared retinal blood flow imaging instrument called the XyCAM RI and XyCAM FC (Vasoptic Medical, Inc., Columbia, MD) in glaucoma management. The main question it aims to answer are: - Can the investigators use blood flow to discriminate between eyes with early-stage glaucoma and variable-matched controls? - Can the investigators validate that the XyCAM FC simultaneously captures both stereo fundus photography and ocular blood flow monitoring? Participants will be - measured for their blood pressure, heart rate, height, and weight - dilated with tropicamide - imaged using the XyCAM RI, fundus photography, optical coherence tomography, and standard automated perimetry - imaged using the XyCAM RI while inhaling 100% oxygen through a mask


Description:

The investigators will capture images of the participant's retina using the XyCAM RI or XyCAM FC ("test data") and by color fundus photography, optical coherence tomography (OCT), and standard automated perimetry (SAP) - the "standard clinical data". The investigators will perform five tests. The first two tests will be conducted using the XyCAM RI or XyCAM FC to obtain "test data". The final two tests will be conducted using routine clinical instruments to obtain "standard clinical data". The investigators will administer eye drops (Tropicamide) to dilate the participant's pupils prior to the first test. Tropicamide is a chemical that causes pupil dilation and is commonly used by doctors to examine the participant's eyes. The entire set of test data sessions should last less than eighty (80) minutes with an additional 60 minutes for carrying out the necessary procedures and imaging using the standard clinical data.


Recruitment information / eligibility

Status Recruiting
Enrollment 150
Est. completion date April 30, 2025
Est. primary completion date December 31, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 88 Years
Eligibility Inclusion Criteria: - Age 18 and older with binocular vision - Able to provide informed consent - Patient is a healthy control OR is recommended for glaucoma assessment OR diagnosed with moderate to severe glaucoma in at least one eye as determined by Hodapp Anderson Criteria Exclusion Criteria: - The subject has significant media opacity (e.g., a visually significant cataract or significant corneal scar) - The subject has previous ocular surgery other than uncomplicated cataract extraction, laser trabeculoplasty (ALT or SLT), or YAG capsulotomy - The subject has prior ocular disease other than glaucoma - The subject has anatomically narrow angles or a prior adverse reaction to administration of Tropicamide or fluorescein dye - The subject has more than 15 diopters of refractive error - The subject is a female who is pregnant or nursing - The subject has diabetes mellitus

Study Design


Related Conditions & MeSH terms


Intervention

Device:
XyCAM with oxygen
After the standard imaging protocols, participants will be asked to inhale 100% oxygen through a mask and will be re-imaged using the XyCAM RI or XyCAM FC.

Locations

Country Name City State
United States University of Maryland Eye Associates at Redwood Baltimore Maryland

Sponsors (3)

Lead Sponsor Collaborator
University of Maryland, Baltimore National Eye Institute (NEI), Vasoptic Medical, Inc

Country where clinical trial is conducted

United States, 

References & Publications (1)

Vinnett A, Kandukuri J, Le C, Cho KA, Sinha A, Asanad S, Thompson G, Chen V, Rege A, Saeedi OJ. Dynamic Alterations in Blood Flow in Glaucoma Measured with Laser Speckle Contrast Imaging. Ophthalmol Glaucoma. 2022 May-Jun;5(3):250-261. doi: 10.1016/j.ogla.2021.10.005. Epub 2021 Oct 18. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Blood flow velocity measure Dynamic video of ocular blood flow through study completion, an average of 1 year
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