Clinical Trials Directory

Trials / Completed

CompletedNCT06501794

Pilot Study: Use of the Saccadometer to Detect Characteristic Saccadic Peak Velocity in Myasthenia Gravis Patients

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
20 (actual)
Sponsor
University of Liverpool · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

Fast eye movements have been shown to demonstrate characteristics that are specific to myasthenia gravis that are not present in other eye movement disorders. It is possible to measure these eye movements and potentially identify these characteristics using new portable eye movement testing equipment. The aim of this pilot study is to discover if these characteristics can be identified using portable eye movement testing equipment in patients with a confirmed diagnosis of myasthenia gravis.

Detailed description

The diagnosis of Myasthenia Gravis (MG) can be challenging, particularly in its ocular manifestation with current clinical procedures. Previous research has shown that fast eye movements in patients suffering with MG have quite specific characteristics that can be used to correctly diagnose the condition. The Saccadometer is a portable eye movement testing device that may provide the ability to detect the characteristics of fast eye movements that Myasthenia patients alone demonstrate - specifically these are hyperfast movements that are present when slower eye movements are impaired by the disease process. These fast movement characteristics are not present in defects of eye movements due to other aetiologies. Saccadic properties of a small group of patients with a confirmed diagnosis of MG will be measured to identify if characteristic hyperfast saccades are present.

Conditions

Interventions

TypeNameDescription
DEVICEQuantitative measurement of eye movementsSaccadometer © - diagnostic device: non-invasive quantitative assessment of eye movement

Timeline

Start date
2016-03-01
Primary completion
2018-03-01
Completion
2018-03-01
First posted
2024-07-15
Last updated
2024-12-18

Source: ClinicalTrials.gov record NCT06501794. Inclusion in this directory is not an endorsement.