Glaucoma, Open-Angle
Conditions
Keywords
choroidal thickness, multifocal electroretinography, optic nerve head, optical coherence tomography, primer open-angle glaucoma
Brief summary
Glaucoma is one of the leading causes of blindness worldwide that is a chronic public health problem. Unfortunately, glaucoma can be diagnosed when the disease reaches a certain level in today's conditions. The aim of this study was to investigate the diagnostic methods that can diagnose glaucoma before it reaches the advanced level and to identify pathophysiological processes. In this study, choroidal thickness was investigated in primary open-angle glaucoma cases and its correlations with OCT and multifocal ERG parameters were evaluated.
Detailed description
In this study, patients with primary open-angle glaucoma who have recently received a new diagnosis with healthy volunteers with age-matched groups were enrolled. All data from 49 glaucoma patients and 47 healthy volunteers were recorded and the study was completed. The study was carried out at the Afyon Kocatepe University Ophthalmology Department between January 2014 and April 2015. Routine ophthalmologic examinations of all participants were performed. Medical treatment was initiated on patients diagnosed with primary open-angle glaucoma. Intraocular pressures and visual acuities of all participants were recorded at baseline, at 1-month, at 3-month, and at 6-month. All participants underwent tests of multifocal electroretinography and the measurements of optic nerve head optical coherence tomography parameters and the choroidal thickness, at the same follow-ups. Visual acuities were measured by using the Snellen chart as the best corrected visual acuity. Intraocular pressures were measured by using applanation tonometry. Choroid thicknesses were also measured and recorded using EDI-OCT mode of optical coherence tomography device (Cirrus HD 4000, Carl Zeiss Meditec AG, Germany). Choroidal thicknesses were measured in three regions: fovea, 3mm nasal and temporal distances of the fovea. The mean of these three measurements was recorded as macular choroidal thickness. The same technician performed all multifocal electroretinography tests of the participants (Metrovision Monpack 3, Metrovision, France). Multifocal electroretinography tests were carried out from a distance of 33 cm using ERG-jet electrode, ground electrode, and a reference electrode. Electrical potential responses from 103 retina regions were recorded. Results were compared statistically and correlations were analyzed (SPSS 20.0, SPSS Inc. IL, USA).
Interventions
Brimonidine tartrate 0.15% 1 eye drop, every day for 6-months
DRUGDorzolamide (as Dorzolamide Hydrochloride) 20 Mg/mL and Timolol (as Timolol Maleate) 5 Mg/mL Eye Drops
Dorzolamide and timolol fixed combination 2 eye drops, every day for 6 months
DRUGBrinzolamide/Timolol 10 MG/1 ML-5 MG/1 ML Ophthalmic Suspension
Brinzolamide and timolol fixed combination 2 eye drops, every day for 6 months
DRUGTravoprost and Timolol
Travoprost and Timolol fixed combination 1 eye drop, every day for 6 months
DRUGBimatoprost and Timolol
Bimatoprost and Timolol fixed combination 1 eye drop, every day for 6 months
DRUGLatanoprost
Latanoprost 0.005% 1 eye drop, every day for 6 months
Sponsors
Afyon Kocatepe University Hospital
Study design
Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Intervention model description
prospective controlled clinical trial
Eligibility
Sex/Gender
ALL
Age
40 Years to No maximum
Healthy volunteers
Yes
Inclusion criteria
for the glaucoma group: * the best corrected visual acuity (BCVA) of 0.6 and above * Intraocular pressure being above 21 mmHg * Detection of open-angle by gonioscopy * Detection of glaucomatous optic disc pitting by fundus examination * Visual field defect in perimetry (Carl Zeiss Meditec AG, Germany)
Exclusion criteria
for the glaucoma group: * A secondary cause of glaucoma * Angle-closure in gonioscopic examination * Corneal opacity or cataract at the level that may affect imaging, vitreous pathology * Intravitreal hemorrhage that may affect fundus appearance, retinal pathology * Chorioretinopathy, optic neuropathy, optic disc pathology, spherical refractive error of 6D and above, cylindrical refraction error of 3D and above and systemic diseases which may affect ocular blood flow Inclusion Criteria for the healthy group: * The best corrected visual acuity (BCVA) of 0.8 and above
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Changes in the mean retinal nerve fiber layer thickness [micrometers] | Baseline, 1-month, 3-month, 6-month | Measuring retinal nerve fiber layer thicknesses \[micrometers\] at 1-month, at 3-month and at 6-month |
| Changes in the mean cup volume [mm3] | Baseline, 1-month, 3-month, 6-month | Measuring cup volume \[mm3\] at 1-month, at 3-month and at 6-month |
| Changes in the mean cup-to-disc ratios | Baseline, 1-month, 3-month, 6-month | Measuring cup-to-disc ratios at 1-month, at 3-month and at 6-month |
| Changes in the mean disc area [mm2] | Baseline, 1-month, 3-month, 6-month | Measuring disc area \[mm2\] at 1-month, at 3-month and at 6-month |
| Macular choroidal thickness measure | Baseline, 1-month, 3-month, 6-month | Measuring macular choroidal thickness at baseline, at 1-month, at 3-month and at 6-month by using optical coherence tomography |
| Changes in multifocal electroretinography parameters (Amplitudes [nv/deg2] and impulse times [ms] of N1, N2 and P1 waves in Ring-1, Ring-2, Ring-3 and Ring-4) | Baseline, 1-month, 3-month, 6-month | Comparison of the mean multifocal electroretinography parameters (Amplitudes \[nv/deg2\] and impulse times \[ms\] of N1, N2 and P1 waves in Ring-1, Ring-2, Ring-3 and Ring-4) at baseline, at 1-month, at 3-month and at 6-month |
| Changes in amplitudes of N1 wave in Ring-1, Ring-2, Ring-3 and Ring-4 [nv/deg2] | Baseline, 1-month, 3-month, 6-month | Comparison of the mean amplitudes of N1 wave \[nv/deg2\] in Ring-1, Ring-2, Ring-3 and Ring-4) at baseline, at 1-month, at 3-month and at 6-month |
| Changes in amplitudes of N2 wave in Ring-1, Ring-2, Ring-3 and Ring-4 [nv/deg2] | Baseline, 1-month, 3-month, 6-month | Comparison of the mean amplitudes of N2 wave \[nv/deg2\] in Ring-1, Ring-2, Ring-3 and Ring-4) at baseline, at 1-month, at 3-month and at 6-month |
| Changes in amplitudes of P1 wave in Ring-1, Ring-2, Ring-3 and Ring-4 [nv/deg2] | Baseline, 1-month, 3-month, 6-month | Comparison of the mean amplitudes of P1 wave \[nv/deg2\] in Ring-1, Ring-2, Ring-3 and Ring-4) at baseline, at 1-month, at 3-month and at 6-month |
| Changes in impulse times of N1 wave in Ring-1, Ring-2, Ring-3 and Ring-4 [ms] | Baseline, 1-month, 3-month, 6-month | Comparison of the mean impulse times of N1 wave \[ms\] in Ring-1, Ring-2, Ring-3 and Ring-4) at baseline, at 1-month, at 3-month and at 6-month |
| Changes in impulse times of P1 wave in Ring-1, Ring-2, Ring-3 and Ring-4 [ms] | Baseline, 1-month, 3-month, 6-month | Comparison of the mean impulse times of P1 wave \[ms\] in Ring-1, Ring-2, Ring-3 and Ring-4) at baseline, at 1-month, at 3-month and at 6-month |
| Changes in P1/N1 ratio of N2 wave in Ring-1, Ring-2, Ring-3 and Ring-4 | Baseline, 1-month, 3-month, 6-month | Comparison of the mean P1/N1 ratios of N2 wave in Ring-1, Ring-2, Ring-3 and Ring-4) at baseline, at 1-month, at 3-month and at 6-month |
| Changes in the mean optic nerve head optical coherence tomography parameters (Retinal nerve fiber layer thickness [micrometers], disc area [mm2], cup-to-disc ratios, cup volume [mm3], neuroretinal rim area [mm2]) | Baseline, 1-month, 3-month, 6-month | Measuring optic nerve head optical coherence tomography parameters (Retinal nerve fiber layer thickness \[micrometers\], disc area \[mm2\], cup-to-disc ratios, cup volume \[mm3\], neuroretinal rim area \[mm2\]) at 1-month, at 3-month and at 6-month |
| Changes in the mean neuroretinal rim area [mm2]) | Baseline, 1-month, 3-month, 6-month | Measuring neuroretinal rim area \[mm2\] at 1-month, at 3-month and at 6-month |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Intraocular pressure measure | Baseline, 1-month, 3-month, 6-month | Measuring intraocular pressure at 1-month, at 3-month and at 6-month |
| Correlations between choroidal thickness and other parameters | Baseline, 6-month | Analyze correlations between changes of choroidal thicknesses and changes of other parameters during the study. |
| Best-corrected visual acuity measure | Baseline, 1-month, 3-month, 6-month | Comparison of the mean best-corrected visual acuities at 1-month, at 3-month and at 6-month |
Outcome results
None listed