Myasthenia Gravis Clinical Trials

Find Myasthenia Gravis Clinical Trials Near You

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

Status: Recruiting
Location: See all (8) locations...
Study Type: Observational
SUMMARY

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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• 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.

Locations
United States
California
UCI Health
RECRUITING
Orange
Illinois
HSHS St. Elizabeth's Hospital
RECRUITING
O'fallon
Kentucky
UK HealthCare - University of Kentucky
RECRUITING
Lexington
New Jersey
Neurology Associates of South Jersey
RECRUITING
Lumberton
South Carolina
Medical University South Carolina
RECRUITING
Charleston
Texas
University of Texas Health Science Center at Houston
RECRUITING
Houston
Other Locations
United Kingdom
University Hospitals Birmingham
RECRUITING
Birmingham
Vitaccess Ltd
RECRUITING
London
Contact Information
Primary
Mark JW Larkin, PhD
mark.larkin@vitaccess.com
+44 1865818983
Time Frame
Start Date: 2024-07-31
Estimated Completion Date: 2034-07
Participants
Target number of participants: 600
Related Therapeutic Areas
Sponsors
Leads: Vitaccess Ltd

This content was sourced from clinicaltrials.gov