Clinical Trials Directory

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.