A Study to Test the Potential of Brillouin Microscopy for Biomechanical Properties Measurements in Human Cornea

Sponsor
Massachusetts General Hospital (Other)
Overall Status
Completed
CT.gov ID
NCT03220529
Collaborator
Massachusetts Eye and Ear Infirmary (Other)
85
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46
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Study Details

Study Description

Brief Summary

The purpose of this research study is to find out if the new Brillouin Ocular Scanner can measure the variation (difference) of the corneal elastic changes involved in the onset of corneal ectasia, induced by LASIK surgery and cornea collagen crosslinking (CXL) treatment. Ectasia refers to the thinning and bulging of the cornea and results in severe vision degradation (loss), which may occur because of a progressive disease (keratoconus) or because of LASIK surgery. It is believed that the structural weakening of the cornea plays a major role in developing ectasia. CXL is a treatment that is able to halt the progression of ectasia.

The Brillouin Ocular Scanner is a technique based on the principles used in the laser speed measuring of a car (radar gun). When laser light illuminates a moving sample, a portion of the light slightly changes color. In our body, e.g in eye and corneal tissue, very weak sound waves are naturally present and they can induce a similar color shift. Measuring this color shift with a sensitive light color meter (spectrometer), we will measure the sound speed in the tissue.

Condition or Disease Intervention/Treatment Phase
  • Device: Brillouin Ocular Scanner
N/A

Study Design

Study Type:
Interventional
Actual Enrollment :
85 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Diagnostic
Official Title:
A Study to Test the Potential of Brillouin Microscopy for Biomechanical Properties Measurements in Human Cornea
Actual Study Start Date :
Nov 1, 2016
Actual Primary Completion Date :
Sep 1, 2019
Actual Study Completion Date :
Sep 1, 2020

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Normal healthy subjects

Healthy subjects with normal appearing corneas respecting all the general inclusion/exclusion criteria. Multiple axial measurements with the Brillouin Ocular Scanner on the cornea will be carried out.

Device: Brillouin Ocular Scanner

Active Comparator: Keratoconus subjects

Subjects classified as patients with mild, moderate, or advanced keratoconus. Multiple axial measurements with the Brillouin Ocular Scanner on the cornea will be carried out.

Device: Brillouin Ocular Scanner

Active Comparator: Subjects diagnosed with PMD

Subjects with Pellucid marginal corneal degeneration (PMD). Multiple axial measurements with the Brillouin Ocular Scanner on the cornea will be carried out.

Device: Brillouin Ocular Scanner

Active Comparator: Patients before and after LASK surgery

Healthy subjects who are scheduled to undergo LASIK surgery. Multiple axial measurements with the Brillouin Ocular Scanner on the cornea will be carried out.

Device: Brillouin Ocular Scanner

Active Comparator: Patients with keratoconus before and after CXL

Subjects who are scheduled to undergo collagen crosslinking treatment. Multiple axial measurements with the Brillouin Ocular Scanner on the cornea will be carried out.

Device: Brillouin Ocular Scanner

Outcome Measures

Primary Outcome Measures

  1. Brillouin frequency shift of corneal stroma [at time of measurement]

    Brillouin frequency shift of corneal stroma in normal corneas and corneas diagnosed with keratoconus and pellucid marginal degeneration

  2. Change of Brillouin frequency shift from base line in corneas received LASIK surgery [1 day and 4-8 weeks]

    Brillouin frequency shift in corneas before and after receiving LASIK surgery

  3. Change of Brillouin frequency shift from base line in corneas received crosslinking treatment [3 days, 1 month, 3 months, 6 months]

    Brillouin frequency shift in corneas before and after receiving crosslinking surgery

Eligibility Criteria

Criteria

Ages Eligible for Study:
15 Years to 75 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Subjects with healthy cornea

  • Patients with mild, moderate, or advanced keratoconus

  • Subjects diagnosed with PMD

  • Patients before and after LASK surgery

  • Patients with keratoconus before and after collagen crosslinking treatment

Exclusion Criteria:
  • Normal volunteer group: presbyopia and/or cataract

  • Keratoconus subjects group: corneas with scars developed, received any ocular surgery, such as laser vision correction surgeries or CXL treatment

  • Subjects diagnosed with PMD: excludes corneas received any ocular surgery, such as laser vision correction or CXL treatment

  • Patients before and after LASK surgery Corneas received priori ocular surgeries, taking any ocular medications except season allergy medicine such as artificial tears

Contacts and Locations

Locations

Site City State Country Postal Code
1 Massachusetts Eye and Ear Infirmary Boston Massachusetts United States 02114
2 Institute for Refractive and Ophthalmic Surgery Zurich Switzerland

Sponsors and Collaborators

  • Massachusetts General Hospital
  • Massachusetts Eye and Ear Infirmary

Investigators

  • Principal Investigator: Seok Hyun Yun, PhD, Massachusetts General Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Seok Hyun Yun, Professor, Massachusetts General Hospital
ClinicalTrials.gov Identifier:
NCT03220529
Other Study ID Numbers:
  • 2015P002404
First Posted:
Jul 18, 2017
Last Update Posted:
Aug 2, 2022
Last Verified:
Jul 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 2, 2022