Utility of Heidelberg Retina Tomograph in Monitoring Glaucoma Progression
NCT ID: NCT00424996
Last Updated: 2014-05-21
Study Results
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Basic Information
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COMPLETED
74 participants
OBSERVATIONAL
2006-08-31
2013-12-31
Brief Summary
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The Heidelberg Retina Tomograph (HRT) is a device that is used to produce a three-dimensional map of the optic nerve and retina, and can be used to detect changes in the optic nerve and retina over time. In previous studies, it has been shown to be useful for the detection of changes due to glaucoma. However, the HRT when compared to other techniques to evaluate the optic nerve such as stereophotography, was found to only somewhat agree.
The current study will compare HRT to stereophotography to determine how good each one is at looking and documenting changes in the optic nerve over time due to glaucoma. Using HRT to initiate early topical medication or to change management requires knowing how well HRT results predict the development of visual loss. Accordingly, the results of this study may affect the management of glaucoma patients by optimizing the follow-up of people with this condition and by initiating appropriate and more individualized treatments. Early treatment is crucial for preventing further visual loss in patients with glaucoma or ocular hypertension (high pressure inside the eye).
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Detailed Description
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However, it has been reported that clinically detectable glaucomatous structural alteration of the ONH may precede the development of reproducible white on white and blue on yellow visual field defects by up to several years.
The HRT is a confocal scanning laser tomography device that creates a three-dimensional topographic analysis of the ONH and the peripapillary retina and includes a statistical analysis to evaluate structural change over time.
This technique showed good sensitivity and high specificity in detecting glaucoma progression when tested using computer simulation. The same good results were obtained by the same authors, in another study, in a small subgroup of 16 patients who were monitored for glaucomatous progression by both HRT and ONH stereophotographs for approximately 5.5 years.
However, in our recent retrospective study, our results demonstrated only fair agreement between HRT and clinical judgment of ONH stereophotographs for progression in glaucoma, for a mean follow-up time with HRT of 2.62 years. Although, the evaluation of the ONH stereophotographs is necessarily subjective, it is widely accepted and has been shown to be effective for evaluating change. Using the stereophotographs assessments as the "reference standard", the HRT sensitivity was 78% and the specificity to 70%. The positive predictive value of the HRT was 47.8%, while the negative predictive value was 90.3%.
According to the results of this study if the frequency of true positives and false positives does not change with longer follow-up, treatment decisions would be based on a test that may be in error 52.2% of the time.
Accordingly, our previous - and other studies - study demonstrated only fair agreement between HRT and clinical judgment of ONH stereophotographs for progression in glaucoma. At present, the available evidence does not appear to be sufficient to show that the addition of HRT improves the ability to predict the development of clinical optic disc change and/or visual field loss.
Therefore the aim of the current study is to investigate the clinical significance of the HRT in monitoring glaucoma progression. In other words we will investigate how well HRT results for glaucomatous progression are able to predict the future development of optic disc and/or visual field changes in patients with OHT and glaucoma.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
* Subjects determined to have OHT or glaucoma
* Spherical refraction within 6.0 D with plus or minus sphere, and cylinder within 3.0 D with plus or minus cylinder
* Subjects that show progression on the HRT
* subjects stable on ONH stereophotographs
* subjects with stable and reliable visual fields
* Subjects willing to make the required visits for the study
* Subjects tolerant to dilating drops
Exclusion Criteria
* Any history of disease or use of medication that may affect visual field reliability
* Past history of stroke or diabetic retinopathy
* Inability of the pupils to be dilated to at least 4 mm for the screening visit
* Inability to undergo either perimetry test or the ophthalmic examination
* Inability to undergo adequate or better quality stereophotographs
20 Years
80 Years
ALL
No
Sponsors
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Glaucoma Research Society of Canada
OTHER
University Health Network, Toronto
OTHER
Responsible Party
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Graham E Trope
DR
Principal Investigators
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Yvonne Buys, MD, FRCSC
Role: PRINCIPAL_INVESTIGATOR
University of Toronto, Department of Ophthalmology; Toronto Western Hospital, Toronto, Ontario, Canada
Graham E Trope, PhD, FRCSC
Role: STUDY_DIRECTOR
University of Toronto, Department of Ophthalmology; Toronto Western Hospital, Toronto, Ontario, Canada
John Flanagan, PhD
Role: STUDY_CHAIR
University of Toronto, Department of Ophthalmology; Toronto Western Hospital, Toronto, Ontario, Canada
Locations
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University of Toronto; Toronto Western Hospital
Toronto, Ontario, Canada
Countries
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References
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Kourkoutas D, Buys YM, Flanagan JG, Hatch WV, Balian C, Trope GE. Comparison of glaucoma progression evaluated with Heidelberg retina tomograph II versus optic nerve head stereophotographs. Can J Ophthalmol. 2007 Feb;42(1):82-8.
Other Identifiers
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UHNToronto
Identifier Type: -
Identifier Source: org_study_id
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