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NCT02014389Recruiting

Evaluation of Objective Perimetry Using Chromatic Multifocal Pupillometer

Objective Perimetry in Normal Subjects,Glaucoma Patients and Retinal Dystrophy Patients

Source: ClinicalTrials.gov · Last updated 25 Apr 2024 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

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.

Status (registry)
Recruiting
Study type
Observational
Enrollment
200 (estimated)
First submitted
12 Dec 2013
Start date
1 Dec 2013
Primary completion date
31 Dec 2026
Lead sponsor
Sheba Medical Center
NCT number
NCT02014389

What you commit to

  • Study type: Observational
  • Planned participants: 200
  • From 1 Dec 2013 to the primary completion date, 31 Dec 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Surgical intraocular ophthalmic procedure within the past 30 days.
  • Synechia of the iris to the lens after surgery or inflammation.
  • Systemic medication that have affect on pupillary reflex .

Other illness

  • Axenfeld-Rieger Syndrome.
  • Iris atrophy (ICE syndrome).
  • Any condition preventing accurate measurement or examination of the pupil.

Other

  • Cloudy corneas.
  • No reactive pupils.
  • Neovascularization.
  • 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.

Who the study is looking for

  • Age 18-80 years old.
  • Signing informed consent.
  • Pupillary reflex to light.

Age in the registry: 18 years to 80 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Sheba medical center
Coordinator of this site? Confirm its status
Tel HaShomerIsraelRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.