Actively Recruiting

Age: 16Years +
All Genders
ID05214612

Predictors and Prognostic Factors of Myasthenia Gravis Outcome

Led by Assiut University · Updated on 2024-07-31

30

Participants Needed

1

Research Sites

12 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are studying myasthenia gravis (MG), a rare autoimmune disease that causes muscle weakness. This study aims to describe different MG subgroups, understand how often they occur, and identify factors that predict how patients respond to treatment. It also seeks to find how common treatment-resistant MG is and to better understand disease relapse and management strategies. The study observes patients with MG who receive drug treatments, including therapies for disease crises like plasmapheresis. It tracks clinical features and treatment responses over time without assigning participants to different treatment groups. The study focuses on changes in muscle strength and quality of life, measured at enrollment and after three months. Participants will undergo assessments including muscle testing, quality of life questionnaires, and monitoring for treatment side effects. Researchers will collect samples and perform imaging and other evaluations related to the disease. The main outcomes are changes in MG-specific scales over three months and the frequency of treatment-related adverse effects. The study started in 2022 and is expected to end in March 2025.

CONDITIONS

Brief Title

Predictors and Prognostic Factors of Myasthenia Gravis Outcome

Who Can Participate

Age: 16Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 16 years and older
  • Includes both males and females
  • Clinical diagnosis of myasthenia gravis confirmed by response to pyridostigmine or nerve stimulation test showing >10% decrement
  • Willingness to undergo sample collection, imaging studies, and other disease-related assessments
Not Eligible

You will not qualify if you...

  • Age younger than 16 years
  • History of chronic psychiatric or neurological disorders other than myasthenia gravis causing weakness or fatigue
  • Severe systemic illness affecting life expectancy

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Monitoring

Duration - 3 months

Participants who receive standard drug treatment for myasthenia gravis and treatment of crisis such as plasmapheresis are observed to assess disease characteristics, treatment outcomes, and quality of life.

Baseline assessment and 3-month follow-up assessment

Trial Site Locations

Total: 1 location

1

Assiut University

Asyut, Egypt, 71515

Actively Recruiting

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Research Team

N

Nourelhoda AA Haridy, Lecturer

E

Eman MH Khedr, Professor

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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Published Research Related To This Trial

Exploring outcomes and characteristics of myasthenia gravis: Rationale, aims and design of registry - The EXPLORE-MG registry.

Rahul Anil, Aditya Kumar, Sneha Alaparthi...

https://pubmed.ncbi.nlm.nih.gov/32388060

Myasthenia gravis: recommendations for clinical research standards. Task Force of the Medical Scientific Advisory Board of the Myasthenia Gravis Foundation of America.

A Jaretzki, R J Barohn, R M Ernstoff...

https://pubmed.ncbi.nlm.nih.gov/10921745