Vitaccess Real MG Registry
Recruiting now
Conditions studied: Myasthenia Gravis
In brief
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 (QoL). The duration of the registry is 10 years from launch, and approximately 600 patients will be recruited in the US and Europe with no defined upper limit. The registry will link relevant patient- and healthcare professional (HCP)-reported data with clinical data from medical records. Patients will be recruited at clinical sites in all participating countries. In the US only, patients can additionally be recruited via community neurologists or direct-to-patient recruitment.
Key facts
- Study ID
- NCT06064461
- Run by
- Vitaccess Ltd
- People needed
- 600
- Starts
- 2024-07-31
- Expected to finish
- 2034-07-01
- Last updated by the study team
- 2025-07-29
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Adult (age ≥18 years) with a clinically-confirmed diagnosis of myasthenia gravis (MG).
- Resident in one of the scope countries.
- Access to a smartphone/tablet/computer/laptop
- Willing and able to provide informed consent in their local language to take part in the study.
You may not qualify if…
- Participation in a clinical trial at the time of study enrolment.
Where it is running
- UCI Health — Orange, California, United States (enrolling)
- HSHS St. Elizabeth's Hospital — O'Fallon, Illinois, United States (enrolling)
- UK HealthCare - University of Kentucky — Lexington, Kentucky, United States (enrolling)
- Neurology Associates of South Jersey — Lumberton, New Jersey, United States (enrolling)
- Medical University South Carolina — Charleston, South Carolina, United States (enrolling)
- University of Texas Health Science Center at Houston — Houston, Texas, United States (enrolling)
- Vitaccess Ltd — London, London, United Kingdom (enrolling)
- University Hospitals Birmingham — Birmingham, United Kingdom (enrolling)
Full record on ClinicalTrials.gov
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