Evaluation of Objective Perimetry Using Chromatic Multifocal Pupillometer
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-80
SponsorSheba Medical Center
About this trial
Objective perimetry can better monitor visual field defects in retinal dystrophy and Glaucoma patients than conventional subjective perimetry. The PLR ( Pupil Light Reflex to short and long wavelength stimuli should be significantly lower compared to healthy participants in areas of visual field defects in retinal dystrophy and Glaucoma patients.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Age 18-80 years old.
Signing informed consent.
Pupillary reflex to light.
Disqualifiers
Cloudy corneas.
Surgical intraocular ophthalmic procedure within the past 30 days.
No reactive pupils.
Synechia of the iris to the lens after surgery or inflammation.
Trial population
Two Groups: 1. Control, 2. Patients - Glaucoma patients with early damage (nasal step) of Humphrey visual field (HVF), Glaucoma patients with advanced damage of HVF (arcuate , tubular vision) and retinal dystrophy patientsl
Trial design
Design model
Case-control
Time perspective
Prospective
Treatments tested in this trial
Not listed
Trial groups
200 Participants
are grouped into 2 trial groupsGroup A: Healthy subjects
Group B: Patients
Trial outcomes
Primary outcomes
1
PLR response amplitude and latency
Time frame
single visitSponsors and contacts
Click on the lead sponsor to view all of their trials.
Source ClinicalTrials.gov