RECRUITING

Vitaccess Real MG Registry

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

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.

Official Title

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

Quick Facts

Study Start:2024-07-31
Study Completion:2034-07
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06064461

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.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Adult (age ≥18 years) with a clinically-confirmed diagnosis of myasthenia gravis (MG).
  2. * Resident in the US, UK, Germany, France, or Italy.
  3. * Access to a smartphone/tablet/computer/laptop
  4. * Willing and able to provide informed consent in their local language to take part in the study.
  1. * Participation in a clinical trial at the time of study enrolment.

Contacts and Locations

Study Contact

Mark JW Larkin, PhD
CONTACT
+44 1865818983
mark.larkin@vitaccess.com

Principal Investigator

Mark JW Larkin, PhD
PRINCIPAL_INVESTIGATOR
Vitaccess Ltd

Study Locations (Sites)

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

Collaborators and Investigators

Sponsor: Vitaccess Ltd

  • Mark JW Larkin, PhD, PRINCIPAL_INVESTIGATOR, Vitaccess Ltd

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-07-31
Study Completion Date2034-07

Study Record Updates

Study Start Date2024-07-31
Study Completion Date2034-07

Terms related to this study

Keywords Provided by Researchers

  • Myasthenia Gravis
  • patient registry
  • longitudinal
  • observational data

Additional Relevant MeSH Terms

  • Myasthenia Gravis