NCT05253534

Brief Summary

Glaucoma is a chronic and progressive optic neuropathy characterized by degeneration of ganglion cells and axons with loss of visual function. It is estimated that glaucoma, which is the second cause of preventable blindness in the world, affects nearly 60 million people worldwide. The most common type of glaucoma is primary open-angle glaucoma (POAG). POAG is a chronic progressive optic neuropathy with characteristic morphological changes in the optic nerve head and retinal nerve fiber. POAG, progressive retinal ganglion cell death and visual field loss are associated with these changes. Risk factors for POAG are age, race, high intraocular pressure (IOP), family history of glaucoma, thin central corneal thickness (CCT), high myopia. IOP is the only modifiable risk factor that we can control. For this reason, the priority in the treatment of POAG has always been to reduce IOP. In glaucoma, the essential point is to preserve the damaged ganglion cell layer and therefore the visual functions. In addition to clinical examination, visual field measurements that measure functions, optical coherence tomography (OCT) thickness measurements that measure anatomical changes, and optic nerve head parameters are the most reliable methods for both diagnosis and evaluation of the efficacy of treatment. Following the results of the visual field and OCT measurements, it will be tried to determine to what extent glaucoma damage can be ceased by the developed GlaucoT glaucoma treatment glasses. In this study, it is aimed to measure the effectiveness and safety of flicker light therapy, the effectiveness of which has been investigated in the treatment of Alzheimer's previously and has clinically significant results, with the GlaucoT glaucoma treatment glasses, which was developed to cease visual field loss with patient comfort at the forefront and at a lower cost.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
15

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Mar 2022

Typical duration for not_applicable

Geographic Reach
1 country

2 active sites

Status
completed

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

First Submitted

Initial submission to the registry

February 2, 2022

Completed
21 days until next milestone

First Posted

Study publicly available on registry

February 23, 2022

Completed
6 days until next milestone

Study Start

First participant enrolled

March 1, 2022

Completed
1.8 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 30, 2023

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 30, 2023

Completed
Last Updated

November 18, 2024

Status Verified

November 1, 2024

Enrollment Period

1.8 years

First QC Date

February 2, 2022

Last Update Submit

November 14, 2024

Conditions

Keywords

GlaucomaNeuroprotectionGamma RhythmNon-invasiveWearable

Outcome Measures

Primary Outcomes (2)

  • Frequency of the adverse events

    In our study, the safety of the GlaucoT glasses with flickering light treatment will be assessed. The purpose of the treatment is to provide neuroprotection with flickering light treatment. The primary outcome for safety of the device is the frequency of the adverse events.

    6 months

  • The stabilization in visual field test

    The second outcome of the clinical trials will be the efficacy of the GlaucoT device. The differences between the patients who use GlaucoT will be compared with the ones that do not use the device under same conditions (e.g. drug use). The assessment will be based on visual field test.

    6 months

Study Arms (2)

Gamma Rhythm Stimulation Group

EXPERIMENTAL

Evaluation of the efficacy and safety of GlaucoT in patients with primary open-angle glaucoma (POAG). In this study, it was planned to investigate the effect of reducing the progression of glaucomatous damage by applying 40 Hz flicker light therapy for 1 hour a day to POAG patients. It is planned to use visual field test, measurements of retinal nerve fiber layer (RNFL) and ganglion cell complex (GCC) layer thicknesses in optical coherence tomography to investigate the effectiveness of the treatment.

Device: GlaucoT Glaucoma Treatment Device

Control Group

NO INTERVENTION

This group will be monitored without using the device.The data will be used only for comparison. Considering the sample size calculations and losses, a total of 60 patients are planned to be included in the study, with 30 patients in each group.

Interventions

In this study, flicker light therapy, the effectiveness of which was investigated in the treatment of glaucoma based on some methods used in different diseases, is described for the first time in glaucoma. Studies investigating the neurodegenerative properties of glaucoma have found similarities in the pathophysiology of Alzheimer's disease and glaucoma. 40 Hz flicker of light Alzheimer 's the positive effects on the knitted cortex have also been shown in studies. 40 Hz flicker light is aimed to reduce glaucoma and retinal ganglion cell loss due to glaucoma, by reducing neurodegeneration by decreasing amyloid and metabolite accumulation by increasing both microglial phagocytic activation effect and retinal blood flow.

Gamma Rhythm Stimulation Group

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Those who have applied to the eye diseases clinic
  • ≥18 years old
  • Those diagnosed with primary open-angle glaucoma (POAG) before the study
  • Recipients of standard drug therapy (defined in diagnostic and treatment guidelines) for POAG
  • Patients deemed appropriate by the investigator to be included in the study after ophthalmological examination
  • Patients who were informed about the study and agreed to participate in the study
  • Those who agree to continue to use acceptable methods of contraception during the study

You may not qualify if:

  • Those with a history of trauma or inflammation in their eyes
  • Those who have undergone intraocular surgery or laser in the last 6 months, excluding those who have had uncomplicated cataract surgery
  • Presence of any retinal or neurological disease other than glaucoma, abnormal ocular motility preventing binocular fixation (eg, nystagmus, strabismus)
  • Those with corneal transplants
  • Advanced disc cupping (c/d ratio 0.8 and above)
  • Large and severe perimetric defects (a central perimetric residual not greater than 10 central degrees)
  • Advanced visual field damage (MD above 12 db)
  • Dry/wet type age-related macular degeneration in one or both eyes
  • Those who have had glaucoma surgery in the past, excluding laser
  • Corneal dystrophies
  • High myopia (more than 6 diopters)
  • Peripheral retinal degenerations with risk of retinal detachment
  • Keratitis
  • Those with severe dry eye syndrome
  • Those with neurological disorders (eg, epilepsy)
  • +5 more criteria

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (2)

Ege University Department of Ophthalmology

Izmir, 35100, Turkey (Türkiye)

Location

Manisa Celal Bayar University Department of Ophthalmology

Manisa, 45030, Turkey (Türkiye)

Location

Related Publications (2)

  • Iaccarino HF, Singer AC, Martorell AJ, Rudenko A, Gao F, Gillingham TZ, Mathys H, Seo J, Kritskiy O, Abdurrob F, Adaikkan C, Canter RG, Rueda R, Brown EN, Boyden ES, Tsai LH. Gamma frequency entrainment attenuates amyloid load and modifies microglia. Nature. 2016 Dec 7;540(7632):230-235. doi: 10.1038/nature20587.

    PMID: 27929004BACKGROUND
  • Samanchi R, Prakash Muthukrishnan S, Dada T, Sihota R, Kaur S, Sharma R. Altered spontaneous cortical activity in mild glaucoma: A quantitative EEG study. Neurosci Lett. 2021 Aug 10;759:136036. doi: 10.1016/j.neulet.2021.136036. Epub 2021 Jun 8.

    PMID: 34116196BACKGROUND

Related Links

MeSH Terms

Conditions

Glaucoma, Open-AngleGlaucoma

Condition Hierarchy (Ancestors)

Ocular HypertensionEye Diseases

Study Officials

  • Ozcan Kayikcioglu, Prof

    Manisa Celal Bayar University Department of Ophthalmology

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
TREATMENT
Intervention Model
PARALLEL
Model Details: Evaluation of the efficacy and safety of GlaucoT in patients with primary open-angle glaucoma (POAG)
Sponsor Type
INDUSTRY
Responsible Party
SPONSOR

Study Record Dates

First Submitted

February 2, 2022

First Posted

February 23, 2022

Study Start

March 1, 2022

Primary Completion

December 30, 2023

Study Completion

December 30, 2023

Last Updated

November 18, 2024

Record last verified: 2024-11

Data Sharing

IPD Sharing
Will not share

Our clinical research protocol will be shared with other researchers. The results of this clinical study will be published in an academical paper.

Locations