Status:
UNKNOWN
Study to Compare Standard Perimetry With the New Scotoma-Oriented Perimetry (SCOPE) Using a New Fast German Adaptive Threshold Estimation (GATE) in Glaucoma Patients
Lead Sponsor:
University Hospital Tuebingen
Collaborating Sponsors:
Alcon Research
Conditions:
Primary Open Angle Glaucoma (POAG)
Eligibility:
All Genders
18+ years
Brief Summary
The purpose of this study is to compare the two psychophysical perimetric techniques regarding progression of the visual field.
Eligibility Criteria
Inclusion
- primary open angle glaucoma (POAG)
- spherical ametropia max. ± 8 dpt
- cylindrical ametropia max. ± 3 dpt
- distant visual acuity \> 10/20
- pupil diameter \> 3 mm
Exclusion
- diabetic retinopathy
- asthma
- 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
- squint
- nystagmus
- albinism
- any ocular pathology, in either eye, that may interfere with the ability to obtain visual fields
- 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
- history or presence of macular disease and/or macular edema, ocular trauma, medications known to affect visual field sensitivity
Key Trial Info
Start Date :
April 1 2010
Trial Type :
OBSERVATIONAL
Allocation :
ESTIMATED
End Date :
December 1 2016
Estimated Enrollment :
12 Patients enrolled
Trial Details
Trial ID
NCT00902109
Start Date
April 1 2010
End Date
December 1 2016
Last Update
February 2 2016
Active Locations (1)
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1
Institute for Ophthalmic Research
Tübingen, Germany, 72076