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  • Stop Retinal Ganglion Cell Dysfunction Study

Stop Retinal Ganglion Cell Dysfunction Study

Principal Investigator

Vittorio Porciatti

Enrollment Status

Closed

Clinical Trial ID

Institutional Protocol # 20140587
National Clinical Trials Identifier NCT02390284

Clinical Trial Summary

Glaucoma is a progressive disease resulting in blindness. Determining the onset of the
disease, predicting its severity and the benefit of pressure lowering eye drops is key to
clinical management aimed at maintaining useful vision with advancing age. This study will
longitudinally monitor a population of glaucoma suspects (with positive factors for the
disease but with normal vision) with noninvasive pattern electroretinogram (PERG) and other
standard eye tests for glaucoma. The PERG measures the function of retinal ganglion cells
(RGCs) that are the parent neurons of the optic nerve. RGCs may become dysfunctional before
dying and their function restored with pressure-lowering eye drops. Glaucoma suspects with
abnormal PERG will be randomized to treatment with eye drops, while those with normal PERG
will be left untreated. All patients will be monitored with PERG, Optic Coherence Tomography
(OCT) and other ancillary tests every 6 months over 4 years.


Phase

Phase 3


Funding Agency/Sponsor

Other


Disease

Glaucoma


Enrollment Eligibility

Inclusion Criteria:
1. Age 18 to 85 years, inclusive
2. Refractive errors within -5 to +3 diopters
3. Best corrected visual acuity (BCVA) better than or equal to 20/30 (Snellen)
4. Normal standard automated perimetry (SAP) according to the Ocular Hypertension
Treatment Study (OHTS) criteria15 (reliability < 15% on all indices, normality > 5% on
all global indices in two consecutive sessions 6 months apart)
5. Minimum untreated Intraocular pressure IOP of 15 mm Hg
6. Glaucoma Suspect Status defined as one or more of the following:
- Glaucomatous optic disc appearance (vertical cup-to-disc ratio [C/D] ≥0.5
- Cup disc ratio asymmetry ≥0.2
- Localized thinning of the disc
- Presence or history of splinter disc hemorrhage
- Moderately increased IOP (>21 to <28 mm Hg).
- Family history of vision loss for glaucoma
Exclusion Criteria:
1. Age-related macular degeneration
2. Diabetes
3. Parkinson's disease
4. Multiple sclerosis
5. Unwilling or unable to give consent, unwilling to accept randomization, or unable to
return for scheduled protocol visits.
6. Pregnant or nursing women.
7. Currently using prescribed pressure lowering medicines and unwilling to be withdrawn
from them.
8. An OHTS risk score high enough in the judgment of the ophthalmologist or optometrist
managing the patient to recommend pressure lowering medicine to the patient and not
randomization.
9. An OCT abnormal enough in a pattern consistent with glaucoma.

Accepts Healthy Volunteers

Call +1 (305) 3266577


Contact Information

Study Contact Vittorio Porciatti
Phone Number +1 (305) 3266577
Email vporciatti@miami.edu
Get detailed information on ClinicalTrials.Gov

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