Age-dependency of Cornea Biomechanics Using OCT Vibrography

Sponsor
Massachusetts General Hospital (Other)
Overall Status
Recruiting
CT.gov ID
NCT03230981
Collaborator
Massachusetts Eye and Ear Infirmary (Other)
90
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1
73
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Study Details

Study Description

Brief Summary

The aim of this pilot study is to assess the ability of a new optical coherence tomography system to obtain information on biomechanics of the cornea.

Condition or Disease Intervention/Treatment Phase
  • Device: Optical imaging of the cornea in healthy subjects
N/A

Detailed Description

The cornea, the clear front window of the eye, consists of finely intertwined collagen fibers, which give the cornea a microstructure that provides mechanical integrity necessary to maintain its typical dome-shape against the intraocular pressure (IOP). Changes in the biomechanical properties can lead to an abnormal corneal shape and refractive errors. As a result, light is not perfectly focused onto the retina and the vision is affected. A typical example of alterations in the cornea's biomechanical properties is found in patients with an eye disorder called Keratoconus, which leads to progressive thinning of the cornea. Numerous studies have shown that promising interventions like collagen crosslinking (CXL) can slow down an arrest progression of ectatic eye diseases. Keratoconus, as a typical example, although it cannot be cured, could be at least halted by CXL. Therefore, early diagnosis of ectasia is crucial for the patient. Current diagnostic methods of ectasia are based on morphological rather than biomechanical analysis. The irregular patterns of the cornea can be detected by pachymetry and topography before clinical signs occur, but these tests cannot reliably differentiate truly weak or keratoconic corneas from atypical normal ones.

These are compelling needs for improved diagnostic methods. More recently, and triggered by those unmet needs, an interest in the mechanical properties of the cornea has emerged. Typical examples of mechanical properties are elastic modulus and corneal stiffness.

In this pilot study the investigators will test the ability of a new OCT Vibrography system to determine cornea material parameters. More precisely, the investigators will study the oscillation response in human corneas in-vivo using a stimulus mechanism used to induce vibrations by touching the surface of the cornea. A localized vibration source paired together with phase-sensitive OCT to measure the frequency response function of the human cornea and to analyze the dependency of the frequency response function on age. Additionally the investigators will use Brillouin Microscopy data for computer simulations to validate OCT Vibrography results.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
90 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Basic Science
Official Title:
Age-dependency of Cornea Biomechanics Measured by OCT Vibrography: A Pilot Study
Actual Study Start Date :
Aug 1, 2019
Anticipated Primary Completion Date :
Sep 1, 2025
Anticipated Study Completion Date :
Sep 1, 2025

Arms and Interventions

Arm Intervention/Treatment
Experimental: Healthy subjects

Optical imaging of the cornea in healthy subjects

Device: Optical imaging of the cornea in healthy subjects
OCT vibrography and Brillouin microscopy

Outcome Measures

Primary Outcome Measures

  1. Number of subjects to successfully complete OCT Vibrography without serious unanticipated adverse events related to application of the device. [1 year]

    Frequency and severity of all treatment-related adverse events

Secondary Outcome Measures

  1. Validation of OCT Vibrography data by means of Brillouin microscopy measurements of the in-vivo cornea [1 year]

    Use of Brillouin microscopy in-vivo data for computer simulations to validate OCT Vibrography results.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 79 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Male or female subjects between the ages of 18 to 79 years

  • Healthy normal subjects with no significant eye disease and no significant refractive errors

Exclusion Criteria:
  • Volunteers with implanted intraocular lenses

  • Volunteers with LASIK or any other eye surgery, and monocular volunteers

  • Volunteers with restricted mobility, who cannot stand up, walk or sit still on a chair without a back

  • Subjects who do not or cannot understand the instructions for imaging

  • Subjects with diabetes, glaucoma family history

  • Subjects who are pregnant and/or breastfeeding.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Massachusetts General Hospital Boston Massachusetts United States 02114

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)

More Information

Publications

Responsible Party:
Seok Hyun Yun, Professor of Dermatology, Massachusetts General Hospital
ClinicalTrials.gov Identifier:
NCT03230981
Other Study ID Numbers:
  • 2017P000867
First Posted:
Jul 27, 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
Keywords provided by Seok Hyun Yun, Professor of Dermatology, Massachusetts General Hospital
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 2, 2022