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
Qualifiers
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 design
Treatments tested in this trial
- Not listed
Trial groups
200 Participants
are grouped into 2 trial groupsSponsors and collaborators
Source ClinicalTrials.gov