NCT07780890

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

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
90

participants targeted

Target at P50-P75 for all trials

Timeline
11mo left

Started Aug 2026

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress13%
Aug 2026Sep 2027

First Submitted

Initial submission to the registry

August 18, 2026

Completed
Same day until next milestone

Study Start

First participant enrolled

August 18, 2026

Completed
6 days until next milestone

First Posted

Study publicly available on registry

August 24, 2026

Completed
1 year until next milestone

Primary Completion

Last participant's last visit for primary outcome

September 1, 2027

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

September 1, 2027

Last Updated

August 25, 2026

Status Verified

August 1, 2026

Enrollment Period

1 year

First QC Date

August 18, 2026

Last Update Submit

August 21, 2026

Conditions

Keywords

corneabiomechanicsbrillouin microscopy

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

Age20 Years - 79 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

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

Study Sites (1)

Massachusetts General Brigham

Boston, Massachusetts, 02114, United States

RECRUITING

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: 33796364BACKGROUND
  • Eltony 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: 35293388BACKGROUND
  • Chow 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

Glaucoma, Open-AngleDry Eye SyndromesKeratoconusCorneal Diseases

Condition Hierarchy (Ancestors)

GlaucomaOcular HypertensionEye DiseasesLacrimal Apparatus Diseases

Study Officials

  • Seok-Hyun Yun, PhD

    Massachusetts General Brigham

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Soyeon (Selina) Ahn, PhD

CONTACT

Seok-Hyun Yun, PhD

CONTACT

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

Locations