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NCT05437003Completed

A Prospective Study to Evaluate the Correlation Between Oculometric Measurements and Clinical Endpoints in PD Patients

A Cross-Sectional Study to Evaluate the Correlation Between Oculometric Measures and MDS-UPDRS in Patients With Idiopathic Parkinson's Disease (PD) and Evaluation of Oculometric Measures in Healthy Participants

Source: ClinicalTrials.gov · Last updated 16 Feb 2024

Brief summary (registry, in English)

This is a prospective study in a cohort of about 500 patients with Idiopathic Parkinson's disease, examined routinely in the neurological outpatient clinic. This study aims to evaluate the correlation between oculometric measures and clinical endpoints. Subjects will be evaluated following a physician examination.The evaluations will include MDS-UPDRS examination, as well as an oculometric evaluation for eye movements. In addition, 500 healthy subjects will be evaluated.

Status (registry)
Completed
Study type
Interventional
Enrollment
465 (actual)
First submitted
23 Jun 2022
Start date
20 Aug 2022
Primary completion date
15 Feb 2024
Lead sponsor
NeuraLight
NCT number
NCT05437003

What you commit to

  • Study type: Interventional
  • Participants enrolled: 465
  • From 20 Aug 2022 to the primary completion date, 15 Feb 2024
  • 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

  • Drug or alcohol abuse
    • Healthy subjects:
  • Drug or alcohol abuse

Other illness

  • Personal or 1st degree relative history of epilepsy
  • Additional neurological diseases
  • Personal or 1st degree relative history of epilepsy
  • Neurological diseases

Other

  • Inability to sit for 20 minutes on a chair in a calm manner
  • Inability to sit for 20 minutes on a chair in a calm manner

Who the study is looking for

  • Men and women with idiopathic PD (Hoehn \& Yahr scale 1-5)
  • Age between 18 and 85 years old
  • Normal or corrected vision
  • Ability to follow instructions
  • Willing and able to sign an informed consent form
  • Age between 18 and 85 years old
  • Normal or corrected vision
  • Ability to follow instructions
  • Willing and able to sign an informed consent form

Criteria the registry did not label

  • PD patients:

Age in the registry: 18 years to 85 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
Rabin Medical Center
Coordinator of this site? Confirm its status
Petah TikvaIsraelUnknown status

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