Brillouin Microscopy Used to Evaluate Corneal Mechanical Properties

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorVienna Institute for Research in Ocular Surgery

About this trial

This study aims to explore the mechanical properties of the cornea using a non-invasive imaging technique called Brillouin microscopy. This innovative method measures corneal elasticity by detecting small shifts in light frequency, which occur due to interactions with acoustic waves in the tissue. These measurements can provide insights into how corneal stiffness is altered in various eye diseases or after surgery.

The study includes 100 participants, divided into different groups: patients with Fuchs' Endothelial Dystrophy (FED), Map Dot Fingerprint Dystrophy (MDFD), and those who have undergone corneal surgeries such as Penetrating Keratoplasty (PKP), Descemet's Stripping Automated Endothelial Keratoplasty (DSAEK), and Descemet Membrane Endothelial Keratoplasty (DMEK). Healthy individuals will also be studied as a control group.

Participants will first receive a standard eye exam, including a slit-lamp examination. Then, Brillouin microscopy will be used to measure the cornea's mechanical stiffness. Additional tests include optical coherence tomography (OCT), corneal topography and tomography, pachymetry (measuring corneal thickness), endothelial cell count, and intraocular pressure (IOP) measurement.

The purpose of this study is to better understand how diseases and surgeries affect corneal biomechanics. The researchers will also examine how well the Brillouin measurements match with findings from other clinical imaging tests. The results may help improve diagnosis and treatment options for corneal disorders.

Eligibility criteria

Qualifiers

Written informed consent prior to surgery

Patients aged 18 years and older

Penetrating Keratoplasty (PKP) and no longer have sutures following PKP o Descemet's Stripping Automated Endothelial Keratoplasty (DSAEK)

Descemet Membrane Endothelial Keratoplasty (DMEK)

Disqualifiers

Patients with inadequate corneal imaging or corneal scarring that would impact results

Patients with other corneal dystrophies or corneal diseases

Patients with active ocular infections or inflammatory conditions

Patients unable to undergo Brillouin imaging adequately

Trial design

Treatments tested in this trial

  • Brillouin optical scanning system (Intelon Optics) (BOSS)

Treatment groups

100 Participants
are divided into 8 treatment groups

8

Treatment groups

See each treatment group below.