Ignite Creation Date:
2024-10-26 @ 3:40 PM
Last Modification Date:
2024-10-26 @ 3:40 PM
Study NCT ID:
NCT06597071
Status:
ENROLLING_BY_INVITATION
Last Update Posted:
None
First Post:
2024-09-11
Brief Title:
Parkinson Atypical Rating of Oculometric Patterns Evaluated Routinely
Sponsor:
None
Organization:
None
Study Overview
Official Title:
Use of Oculometric Measures in the Differential Diagnosis of Typical and Atypical Parkinsonian Conditions a Pilot Study
Status:
ENROLLING_BY_INVITATION
Status Verified Date:
2024-09
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
No
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
PARATROOPER
Brief Summary:
This is an observational cross-sectional study in 4 cohorts of patients with parkinsonian syndromes and healthy subjects who are visiting the Movement Disorders outpatient clinics
The aim of the study is to assess the difference of oculometric measures in different neurodegenerative brain conditions and their accuracy as compared to clinical diagnosis in order to find a correlation with accepted clinical endpoints in subjects who meet the inclusion criteria and who provide a signed Informed Consent
The aim of the study is to assess the difference of oculometric measures in different neurodegenerative brain conditions and their accuracy as compared to clinical diagnosis in order to find a correlation with accepted clinical endpoints in subjects who meet the inclusion criteria and who provide a signed Informed Consent
Detailed Description:
As a part of the study about 40 subjects will undergo a neurological evaluation including motor and cognitive assessments and a NeuraLight session including oculometric measurements and eye-tracking recordings using a novel software-based platform and an eye-tracking system Tobii CE-marked class B approved device Test duration will be approx 30 minutes The oculometric evaluation will occur at baseline and all subjects will be recruited over a period of 9 months All assessments will be performed during a clinic visit unless authorized to be conducted remotely
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
None
Is a FDA Regulated Device?:
None
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None