Status:

COMPLETED

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

Lead Sponsor:

University of Liverpool

Collaborating Sponsors:

Liverpool University Hospitals NHS Foundation Trust

Conditions:

Myasthenia Gravis

Eligibility:

All Genders

18+ years

Phase:

NA

Brief 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 movem...

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 s...

Eligibility Criteria

Inclusion

  • Patient participants
  • Confirmed diagnosis of Myasthenia Gravis by either a positive acetylcholine antibody serum test (AChR) and/or a positive single fibre electromyograph (SFEMG) test.
  • Patient participants must have also had at least one episode of diplopia and/or eye movement abnormality attributed to their diagnosis of MG.
  • Healthy participants:
  • Must have no history of eye movement abnormality
  • No have no history of other auto-immune disease (specifically diabetes, Thyroid Eye Disease and Chronic External Ophthalmoplegia).

Exclusion

  • Patients without confirmed Myasthenia Gravis diagnosis by means of either a positive AChR serum test and/or a positive SFEMG test.
  • Patients with confirmed Myasthenia Gravis who have not had at least one episode of diplopia and or ptosis.
  • Patients with current or previous episodes of ocular motility dysfunction that have a confirmed diagnosis other than Myasthenia Gravis.
  • Any healthy participant found to have an abnormality of vision or eye movement upon screening or a history of auto-immune disease.

Key Trial Info

Start Date :

March 1 2016

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

March 1 2018

Estimated Enrollment :

20 Patients enrolled

Trial Details

Trial ID

NCT06501794

Start Date

March 1 2016

End Date

March 1 2018

Last Update

December 18 2024

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