RECRUITING

Vitaccess Real MG Registry

Description

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.

Study Overview

Study Details

Study overview

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.

Vitaccess Real MG Registry: A Prospective International Observational Patient Registry in Myasthenia Gravis Linking Clinical and Patient-reported Data.

Vitaccess Real MG Registry

Condition
Myasthenia Gravis
Intervention / Treatment

-

Contacts and Locations

O'Fallon

HSHS St. Elizabeth's Hospital, O'Fallon, Illinois, United States, 62269

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * Adult (age ≥18 years) with a clinically-confirmed diagnosis of myasthenia gravis (MG).
  • * Resident in the US, UK, Germany, France, or Italy.
  • * Access to a smartphone/tablet/computer/laptop
  • * Willing and able to provide informed consent in their local language to take part in the study.
  • * Participation in a clinical trial at the time of study enrolment.

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

Vitaccess Ltd,

Mark JW Larkin, PhD, PRINCIPAL_INVESTIGATOR, Vitaccess Ltd

Study Record Dates

2034-07