A Study to Assess Brillouin Hydration Mapping for the Evaluation of Ocular Tissues and Diseases
2 other identifiers
observational
90
1 country
1
Brief Summary
The overall goal of this study is to develop Brillouin microscope as a novel tool for measuring biomechanical and hydration properties of human tissues in vivo.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Aug 2026
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
August 18, 2026
CompletedStudy Start
First participant enrolled
August 18, 2026
CompletedFirst Posted
Study publicly available on registry
August 24, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
September 1, 2027
ExpectedStudy Completion
Last participant's last visit for all outcomes
September 1, 2027
August 25, 2026
August 1, 2026
1 year
August 18, 2026
August 21, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Number of subjects to successfully complete Brillouin measurement without serious unanticipated adverse events related to application of the device.
Number and percentage of enrolled subjects who complete the single Brillouin imaging session without experiencing a serious unanticipated adverse event related to the investigational Brillouin Ocular Scanner, as determined by study staff monitoring during and immediately following the imaging procedure.
Through completion of the single study visit, approximately 1-2 hours
Study Arms (2)
Control Group
Healthy Subjects
Patient Group
Patient Subjects (Fuch's endothelial dystrophy, Corneal guttae, Open-angle glaucoma, Dry eye disease, Keratoconus, post-LASIK)
Eligibility Criteria
Aim 1 - Control Group (Healthy Subjects) : 10 subjects per 6 age ranges (20-29yr, 30-39yr, 40-49yr, 50-59yr, 60-69yr, 70-79yr), total 60 subjects Aim 2 - Patient Groups : 20 patients per 6 diseases (Moderate Fuchs' endothelial dystrophy, Early-stage isolated corneal guttae, Primary open-angle glaucoma, Dry eye disease, Keratoconus, post-LASIK), total 120 patients.
You may qualify if:
- Healthy volunteers with normal eyes
- Visual acuity between +2 to -6 diopters
You may not qualify if:
- History of refractive or cataract surgery
- History of ocular disease
- Active non-ophthalmic systemic disease
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Massachusetts General Hospitallead
- National Eye Institute (NEI)collaborator
- Massachusetts Eye and Ear Infirmarycollaborator
Study Sites (1)
Massachusetts General Brigham
Boston, Massachusetts, 02114, United States
Related Publications (3)
Ryu S, Martino N, Kwok SJJ, Bernstein L, Yun SH. Label-free histological imaging of tissues using Brillouin light scattering contrast. Biomed Opt Express. 2021 Feb 17;12(3):1437-1448. doi: 10.1364/BOE.414474. eCollection 2021 Mar 1.
PMID: 33796364BACKGROUNDEltony AM, Shao P, Yun SH. Measuring mechanical anisotropy of the cornea with Brillouin microscopy. Nat Commun. 2022 Mar 15;13(1):1354. doi: 10.1038/s41467-022-29038-5.
PMID: 35293388BACKGROUNDChow DM, Yun SH. Pulsed stimulated Brillouin microscopy. Opt Express. 2023 Jun 5;31(12):19818-19827. doi: 10.1364/OE.489158.
PMID: 37381389BACKGROUND
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Seok-Hyun Yun, PhD
Massachusetts General Brigham
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Professor
Study Record Dates
First Submitted
August 18, 2026
First Posted
August 24, 2026
Study Start
August 18, 2026
Primary Completion (Estimated)
September 1, 2027
Study Completion (Estimated)
September 1, 2027
Last Updated
August 25, 2026
Record last verified: 2026-08
Data Sharing
- IPD Sharing
- Will not share