Actively Recruiting
Evaluation of Objective Perimetry Using Chromatic Multifocal Pupillometer
Led by Sheba Medical Center · Updated on 2024-04-25
200
Participants Needed
1
Research Sites
682 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Evaluation of Objective Perimetry Using Chromatic Multifocal Pupillometer
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 18-80 years old.
- Signing informed consent.
- Pupillary reflex to light.
You will not qualify if you...
- 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.
- Neovascularization.
- Axenfeld-Rieger Syndrome.
- Iris atrophy (ICE syndrome).
- Iris coloboma.
- Sphincter damage due to ischemia.
- Sphincter damage due to trauma (tears of sphincter or diffuse damage to muscle).
- Sphincter damage due to Herpes Zoster Uveitis.
- Sphincter damage due to high intraocular pressure.
- Iris tumor or cyst.
- Ectropion uvae.
- Adie's pupil.
- Third nerve aberrant regeneration of the iris sphincter.
- RP patients with Optic neuropathy with the potential of producing a positive RAPD (Relative Afferent Pupillary Defect).
- Chronic use of myotics or mydriatics.
- Systemic medication that have affect on pupillary reflex .
- Any condition preventing accurate measurement or examination of the pupil.
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Sheba Medical Center
Tel Litwinsky, Israel, 52621
Actively Recruiting
Research Team
Y
Ygal Rotenstreich, MD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
Not the Right Trial for You?
Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.
Already have an account? Log in here