NCT04001582

The United Kingdom Facioscapulohumeral Muscular Dystrophy Patient Registry

The UK Facioscapulohumeral Muscular Dystrophy Patient Registry

• Status: Recruiting
• Phase: —
• Study type: Observational
• Enrollment: 1,018 (estimated)
• Sponsor: Newcastle University · Academic / Other
• Sex: All
• Age: —
• Healthy volunteers: Not accepted

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.

Detailed description

The UK FSHD Patient Registry (https://www.fshd-registry.org/uk/) recruits any individual, from anywhere within the United Kingdom, with a diagnosis of FSHD. The registry is sponsored by Muscular Dystrophy UK. Participants may be referred to the registry by health care professionals, genetic testing/laboratory centres who are aware of the registry etc. Alternatively, a participant may have discovered the registry via promotional activities or by their own online searches. After completing the consent process, participants are able to enter information on to the registry platform (note all forms are available to view on the registry website before joining the registry). This is an ongoing database and all participants are invited to update their information on an annual basis. The database is designed to be self reporting, however where specialised clinical or genetic information is required, the neuromuscular specialist in charge of the participants care can be invited to provide some additional information. The participant is able to select a health care provider from a pre-populated list at registration stage, if they wish to (optional feature). This information is included in the patient information and consent. Relevant R\&D approval has been recieved.

Conditions

• Facioscapulohumeral Muscular Dystrophy

Interventions

Type	Name	Description
OTHER	Patient Registry	Participants who have volunteered to participate will complete various questionnaires relating to their condition.

Timeline

• Start date: 2013-05-01
• Primary completion: 2040-01-01
• Completion: 2040-01-01
• First posted: 2019-06-28
• Last updated: 2024-05-09

Locations

1 site across 1 country: United Kingdom