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The United Kingdom Facioscapulohumeral Muscular Dystrophy Patient Registry
Sponsor: Newcastle University
Summary
Facioscapulohumeral Dystrophy (FSHD) is the third most common form of neuromuscular dystrophy worldwide with an estimated prevalence of one in 20,000. FSHD is an autosomal dominant genetic disease and is estimated to affect up to 3,000 people in the UK. The patient registry facilitates a questionnaire based research study to better characterise and understand the disease in the UK, and helps to identify potential participants eligible for clinical trials.
Official title: The UK Facioscapulohumeral Muscular Dystrophy Patient Registry
Key Details
Gender
All
Age Range
Any - Any
Study Type
OBSERVATIONAL
Enrollment
1018
Start Date
2013-05
Completion Date
2040-01
Last Updated
2024-05-09
Healthy Volunteers
No
Conditions
Interventions
Patient Registry
Participants who have volunteered to participate will complete various questionnaires relating to their condition.
Locations (1)
John Walton Muscular Dystrophy Research Centre
Newcastle upon Tyne, United Kingdom