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NCT04107610

Normative Oculomotor and Vestibular Data in Pediatric Population

Status unknown NA Last updated 3 March 2021
What this trial tests

NA trial testing I-PAS in Healthy in 600 participants. Status unknown.

Timeline
1 April 2021
Primary endpoint
31 January 2022
31 August 2022

Quick facts

Lead sponsorNeurolign
PhaseNA
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposeother
Enrollment600
Start date1 April 2021
Primary completion31 January 2022
Estimated completion31 August 2022
Sites2 locations across United States

Drugs / interventions tested

Conditions studied

Sponsor

Neurolign

Who can join

Adults 6 to 18, any sex, with Healthy. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this study is to use a device called I-Portal® Portable Assessment System (I-PAS) to record eye movements in response to a number of visual and auditory stimuli designed to evaluate neural brain pathways related to oculomotor, vestibular, reaction time and cognitive (OVRT-C) development. The goal of this research is to collect normative data for the OVRT-C tests from a healthy pediatric population.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Healthy

Currently open trials in the same condition.

Other Neurolign trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04107610.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing