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N/A N=180

Variability in Perimetry Study

Glaucoma

Enrolled (actual)
180
Serious AEs
0.0%
Results posted
Feb 2017
Primary outcome: Primary: Number of Subjects Progressing in Each Group Using Pointwise Linear Regression — 0; 0 participants — p=.21

Study Design & Population

Study type
Observational
Phase
N/A
Interventions
Comparison of four visual field testing strategies (Procedure)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
VA Office of Research and Development
Primary completion
Sep 2015

Outcome Measures

OutcomeResultp-value
PRIMARY
Number of Subjects Progressing in Each Group Using Pointwise Linear Regression
0; 0 .21

Summary

Improved Assessment of Visual Field Change is a trial aimed at investigating mechanisms of visual field testing variability. The investigators have found using larger stimulus size substantially lowers short-term variability. In this study, the investigators will determine if larger stimuli detect visual field change at an earlier time. The investigators are also developing a statistical model that accounts for correlations of neighboring test locations.

Eligibility Criteria

Inclusion Criteria

  • Mean deviation of -20 or better with 5-8 points (optimally 10 points) with a value of p= 0.05 or better on the total deviation plot
  • Mild cataract with VA of 20/30 or better pinholed
  • Refractive error of = to or less than 6 diopters with = or less than 3.50 diopters of cylinder
  • Pupil diameter of 3 mm minimum
  • Controlled hypertension, diabetes, migraine
  • Pseudophakic/refractive surgery if no vision problems
  • Trabeculectomy okay

Exclusion Criteria

  • History of other ocular or neurologic disease or surgery
  • History of stroke
  • Systemic disease [lupus, graves, cancer (within the last 5 yrs), AIDS, other]
  • History of amblyopia
  • Unreliable patient
  • Frequently misses appointments
  • Tests poorly
  • Ocular hypertension
  • Retinal problems
  • Diabetic retinopathy
  • Neurological disease (IIH, ON, AION)
  • Cancer not in remission for the last 5 years
  • Vein or artery occlusions
  • Macular degeneration
  • Trauma with vision loss
  • Ocular inflammation (pars planitis, iritis, temporal aeuritis)
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT01051739). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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