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RECRUITINGOBSERVATIONAL

Clinical Evaluation of Visual Field Change in Glaucoma: an Assessment of Different Models of Progression

An Observational Prospective Longitudinal Study for the Clinical Evaluation of Visual Field Change in Glaucoma. An Assessment of Different Models of Progression

Important: This information is not medical advice. Talk to your doctor about whether a clinical trial is right for you.

About This Trial

The purpose of this observational study is to collect over time a series of data in patients with glaucoma in order to evaluate different approaches in defining the progression of this pathology. These data will be collected in repeated visits over a 36-months follow-up period. At each visit, the COMPASS fundus perimeter and the Humphrey Field Analyzer (HFA) perimeter will be used to assess retinal functionality; an Optical Coherence Tomography (OCT) examination will also be performed to evaluate and obtain clinical information about the structure of the retina.

Who May Be Eligible (Plain English)

Who May Qualify: - Glaucomatous optic nerve head in both eyes; - Age between 40 and 90 years; - Best Corrected Visual Acuity ≤ 0.3 \[logMar\]; - Spherical refraction between -6D and +6D; - Astigmatism between -2D and +2D. Who Should NOT Join This Trial: - Any ocular surgery, except for: uncomplicated cataract surgery and/or glaucoma surgery in both eyes performed within 6 months before enrollment; - Any ocular pathology that can affect visual field other than glaucoma; - Use of any drug that can interfere with the correct execution of perimetry or that would produce visual field loss; - Inability to obtain reliable perimetric examinations; - Patients with advanced glaucoma for whom, according to the clinician, a 24-2 grid is not advisable to correctly monitor the patient. Always talk to your doctor about whether this trial is right for you.

Original Eligibility Criteria

View original clinical language
Inclusion Criteria: * Glaucomatous optic nerve head in both eyes; * Age between 40 and 90 years; * Best Corrected Visual Acuity ≤ 0.3 \[logMar\]; * Spherical refraction between -6D and +6D; * Astigmatism between -2D and +2D. Exclusion Criteria: * Any ocular surgery, except for: uncomplicated cataract surgery and/or glaucoma surgery in both eyes performed within 6 months before enrollment; * Any ocular pathology that can affect visual field other than glaucoma; * Use of any drug that can interfere with the correct execution of perimetry or that would produce visual field loss; * Inability to obtain reliable perimetric examinations; * Patients with advanced glaucoma for whom, according to the clinician, a 24-2 grid is not advisable to correctly monitor the patient.

Locations (2)

Clinica oculistica Ospedale San Paolo
Milan, Milano, Italy
Glaucoma Research Center, IRCCS Fondazione "G.B. Bietti"
Roma, Roma, Italy