Comparison of Visual Fields: Humphrey Field Analyzer (HFA) SITA Strategy, SCOPE (GATE Strategy) and Humphrey MATRIX Perimeter

NCT ID: NCT01068938

Last Updated: 2016-12-20

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

30 participants

Study Classification

OBSERVATIONAL

Study Start Date

2008-11-30

Study Completion Date

2016-12-31

Brief Summary

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The purpose of this study is to compare three perimetric techniques regarding progression of the visual field.

Detailed Description

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Conditions

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Glaucoma

Keywords

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visual field perimetry glaucoma progression grid POAG and glaucoma suspects with prostaglandin monotherapy

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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open angle glaucoma, glaucoma suspects

risk of progression, Latanoprost monotherapy

three different perimeters: HFA, Octopus, MATRIX

Intervention Type DEVICE

visual fields

Interventions

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three different perimeters: HFA, Octopus, MATRIX

visual fields

Intervention Type DEVICE

Eligibility Criteria

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Inclusion Criteria

* max. ± 8 dpt sph, max. ± 3 dpt cyl
* distant visual acuity \> 10/20
* isocoria, pupil diameter \> 3 mm
* at least one risk of progression: optic disc (splinter) hemorrhage / cup to disc ratio (CDR) \> 0.7 / inter-eye asymmetry of CDR \>0.2 / notching of the optic disc /retinal nerve fibre layer (RNFL) defects / intraocular pressure( IOP) \>22 mmHg / central corneal thickness \< 520 µm / advanced visual field defect stage Aulhorn III / elder than 70 years

Exclusion Criteria

* pregnancy, nursing
* diabetic retinopathy
* asthma
* HIV+ or AIDS
* history of epilepsy or significant psychiatric disease
* medications known to effect visual field sensitivity
* infections (e.g. keratitis, conjunctivitis, uveitis)
* severe dry eyes
* miotic drug
* amblyopia
* squint
* nystagmus
* albinism
* any ocular pathology, in either eye, that may interfere with the ability to obtain visual fields,disc imaging or accurate IOP readings
* keratoconus
* intraocular surgery (except for uncomplicated cataract surgery) performed \< 3 month prior to screening
* history or signs of any visual pathway affection other than glaucoma
* allergies with regard to topic glaucoma medication
* history or presence of macular disease and / or macular edema
* ocular trauma
* medications known to affect visual field sensitivity
Minimum Eligible Age

18 Years

Maximum Eligible Age

99 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Pfizer

INDUSTRY

Sponsor Role collaborator

University Hospital Tuebingen

OTHER

Sponsor Role lead

Responsible Party

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Ulrich Schiefer

Prof. Dr. med.

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Ulrich Schiefer, MD

Role: PRINCIPAL_INVESTIGATOR

Centre for Ophthalmology, Institute for Ophthalmic Research

Locations

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Centre for Ophthalmology, Institute for Ophthalmic Research

Tübingen, , Germany

Site Status

Countries

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Germany

References

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Schiefer U, Pascual JP, Edmunds B, Feudner E, Hoffmann EM, Johnson CA, Lagreze WA, Pfeiffer N, Sample PA, Staubach F, Weleber RG, Vonthein R, Krapp E, Paetzold J. Comparison of the new perimetric GATE strategy with conventional full-threshold and SITA standard strategies. Invest Ophthalmol Vis Sci. 2009 Jan;50(1):488-94. doi: 10.1167/iovs.08-2229. Epub 2008 Dec 5.

Reference Type BACKGROUND
PMID: 19060285 (View on PubMed)

Related Links

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Other Identifiers

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116MIR08023

Identifier Type: OTHER_GRANT

Identifier Source: secondary_id

428/2008BO1

Identifier Type: OTHER

Identifier Source: secondary_id

X-SCOPE

Identifier Type: -

Identifier Source: org_study_id