Clinical Trials Directory

Trials / Completed

CompletedNCT03966560

Choroidal Thickness and Its Correlations With Ocular Parameters in Primary Open-angle Glaucoma

Choroidal Thickness and Its Correlations With Ocular Parameters in Cases With Primary Open-angle Glaucoma

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
96 (actual)
Sponsor
Afyon Kocatepe University Hospital · Academic / Other
Sex
All
Age
40 Years
Healthy volunteers
Accepted

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).

Conditions

Interventions

TypeNameDescription
DRUGBrimonidine TartrateBrimonidine 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 DropsDorzolamide and timolol fixed combination 2 eye drops, every day for 6 months
DRUGBrinzolamide/Timolol 10 MG/1 ML-5 MG/1 ML Ophthalmic SuspensionBrinzolamide and timolol fixed combination 2 eye drops, every day for 6 months
DRUGTravoprost and TimololTravoprost and Timolol fixed combination 1 eye drop, every day for 6 months
DRUGBimatoprost and TimololBimatoprost and Timolol fixed combination 1 eye drop, every day for 6 months
DRUGLatanoprostLatanoprost 0.005% 1 eye drop, every day for 6 months

Timeline

Start date
2014-01-01
Primary completion
2015-01-01
Completion
2015-04-01
First posted
2019-05-29
Last updated
2019-05-29

Regulatory

Source: ClinicalTrials.gov record NCT03966560. Inclusion in this directory is not an endorsement.