The Vitaccess Real MG Registry

Clinicians

Registry overview

Design

Vitaccess Real MG (VRMG) is a patient registry designed to capture longitudinal observational data on myasthenia gravis (MG), its treatment, and impact on symptoms, daily activities, and quality of life. The registry links direct patient-reported data with data reported by healthcare professionals (HCPs) and data from patients’ medical records.

Eligibility criteria

Adults who are 18 years or older, with a confirmed diagnosis of MG and living in the United States or United Kingdom are currently eligible to participate in VRMG. To take part in the registry, potential participants should also have access to a smartphone, tablet, computer or laptop, and be willing and able to provide informed consent in their local language. Patients participating in a clinical trial at the time of registry enrolment will not be eligible. 

Duration

The registry will run for up to 10 years.

ClinicalTrials.gov

(NCT06064461)

Site recruitment

Countries
Medical record data
Patient-reported outcomes data
  • United States
  • United Kingdom (England or Scotland only)

Electronic case report form (eCRF) data will be entered by designated healthcare professionals based at the site​

Participants will complete patient-reported outcome measures on the Vitaccess Real MG Registry platform, which they can access on their own device (smartphone, tablet, computer, or laptop). The surveys will include questions on MG symptoms, its treatment, and its impact on quality of life.​

Community recruitment

Countries
Medical record data
Patient-reported outcomes data

United States

Electronic case report form (eCRF) data will be captured via an electronic medical record aggregator.

Participants will complete patient-reported outcome measures on the Vitaccess Real MG Registry platform, which they can access on their own device (smartphone, tablet, computer, or laptop). The surveys will include questions on MG symptoms, its treatment, and its impact on quality of life.​

Sponsor and Scientific Advisory Board

Dr Ali Habib

Dr Ali Habib

UCI Health, CA

Prof Saiju Jacob

Prof Saiju Jacob

Birmingham University Hospital

Dr Francesco Saccà

Dr Francesco Saccà

University of Naples

Dr Zabeen Mahuwala

Dr Zabeen Mahuwala

UK HealthCare, KY

Dr Kelly Gwathmey

Dr Kelly Gwathmey

VCU Health

Emma Ward

Emma Ward

Patient representative, UK

Amanda Hayes

Amanda Hayes

Muscular Dystrophy UK

MGFA

MGFA

Partner

Vitaccess

Vitaccess

Sponsor

Join our network

We are currently inviting practicing neurologists in the United States who are treating MG patients in the community to join the registry and contribute to patient recruitment. ​

If you join our network, you will:​

  • Invite eligible patients to join the registry​
  • Be compensated when you complete training and for each patient you recruit. ​

You will not:​

  • Be required to complete the informed consent process with your patients (they will complete this process independently)​
  • Provide any data about your patients.​

If you are interested, you will be required to complete a 5-step onboarding process.

Step 1

Review and sign a Confidentiality Disclosure Agreement

Step 2

Complete a feasibility questionnaire

Step 3

Review and sign an agreement

Step 4

Complete a 1-hour virtual training session

Step 5

Start recruiting patients and getting compensated

    Please select all that apply

    I am based in the United States
    I am a practicing neurologist treating MG patients in the community
    I currently treat MG patients who would be eligible to participate in the VRMG registry
    I have valid proof of my credentials (e.g., GCP/ICH training) to provide

    Please enter your contact details and our team will be in touch.




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