Trials / Completed
CompletedNCT01021982
Evaluation of Objective Perimetry Using Pupillometer
Objective Perimetry in Normal Subjects,Glaucoma Patients and Retinitis Pigmentosa Patients .
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 60 (actual)
- Sponsor
- Sheba Medical Center · Other Government
- Sex
- All
- Age
- 18 Years – 75 Years
- Healthy volunteers
- Accepted
Summary
Objective perimetry can better monitor visual field defects in RP and Glaucoma patients than conventional subjective perimetry.The PLR ( Pupil Light Reflex ) of the short and long wave ratio should be significantly higher in areas of visual field defects in RP and Glaucoma patients.
Detailed description
Pupil light reflex will be measured by a pupillometer in response to short and long wavelength light small spot stimulus in different area of the visual field. The PRL will be measured in four quadrant, central, 10, 20, and 30 degree from the visual axis. Stimulus duration will be 1000 ms (1 sec), with intervals of 890 ms between stimuli. The stimuli size V with light intensity of 39.8 cd-s/m2 for both short wavelength stimuli (peak 485 nm) and long wavelength stimuli (peak 620nm).
Conditions
Timeline
- Start date
- 2009-11-01
- Primary completion
- 2013-01-01
- Completion
- 2013-01-01
- First posted
- 2009-12-01
- Last updated
- 2014-11-19
Locations
1 site across 1 country: Israel
Source: ClinicalTrials.gov record NCT01021982. Inclusion in this directory is not an endorsement.