Muscular Dystrophy, Facioscapulohumeral

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Review clinical trials related to Muscular Dystrophy, Facioscapulohumeral. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Motor Outcomes to Validate Evaluations in Pediatric FSHD (MOVE Peds)

The primary goal of this study is to validate motor and functional outcomes and refine clinical trial strategies for pediatric-onset FSHD

Participants needed: 80
Trial details
Age: 5-17Biological sex: AllType: ObservationalSponsor: University of Kansas Medical CenterUpdated: Feb 25, 2026Locations: 7
Eligibility criteria

Age 5-17 years. [+3]

Unwilling or unable to provide informed consent or assent. Any other medical con... [+7]

Status: Recruiting

Clenbuterol to Target DUX4 in FSHD

The purpose of this study is to determine if Clenbuterol is a therapeutic option for FSHD by determining the safety and tolerability of the medication at three different dose levels.

Participants needed: 30
Trial details
Phase: Phase 1Age: 18-75Biological sex: AllType: InterventionalSponsor: Jeffrey StatlandUpdated: Feb 25, 2026Locations: 3
Eligibility criteria

Genetically confirmed diagnosis of FSHD type 1 or 2, or have a clinical diagnosi... [+6]

Pregnant or planning to become pregnant during the conduct of the study [+8]

Status: Recruiting

BetterLife FSHD: A Patient-driven Health and Research Platform

BetterLife FSHD is a registry platform built to support people living with FSHD. It connects patients with personalized resources, tools, and research opportunities that match their health experiences and needs. At the same time, BetterLife collects secure health and experience data from patients to support research. This data is shared with researchers to help better understand FSHD and work toward improved care, treatments, and outcomes for the community. Learn more and enroll at: www.BetterLifeFSHD.org

Participants needed: 5,000
Trial details
Age: 1+Biological sex: AllType: ObservationalSponsor: FSHD SocietyUpdated: Feb 20, 2026Locations: 1Duration: 100 Years
Eligibility criteria

Individuals with a clinical or genetic diagnosis of FSHD, or individuals with a... [+4]

Individuals residing outside the United States or its territories [+1]

Status: Recruiting

Magnetic Resonance Imaging and Ultrasound Comparison With Load Evaluation

Facioscapulohumeral dystrophy (FSHD) is one of the most common hereditary neuromuscular disorders (NMD), with an estimated prevalence of 2000 patients in the Netherlands. Magnetic resonance imaging (MRI) and muscle ultrasound have contributed to an enhanced understanding of the pathophysiology of Facioscapulohumeral Muscular Dystrophy (FSHD). Previously, our group demonstrated the potential presence of an intermediate factor between muscle fiber loss and clinical weakness in FSHD. The influence of disrupted muscle architecture in FSHD on muscle contractile efficiency is a likely candidate for this factor, and remains relatively unexplored. In this study, we aim to assess the use of ultrasound-defined contractile performance, in comparison with current measures including structural MRI, for monitoring disease progression in FSHD.

Participants needed: 100
Trial details
Age: 18-70Biological sex: AllType: ObservationalSponsor: Radboud University Medical CenterUpdated: Jan 13, 2025Locations: 1
Eligibility criteria

Age between 18 and 70 years. [+3]

BMI ≥ 35 [+12]

Status: Recruiting

Disease Burden and Living Situation of Patients With Facioscapulohumeral Muscular Dystrophy

The goal of this observational study is to learn the patient journey, disease burden, living situation, quality of life and etc. in patients with Facioscapulohumeral Muscular Dystrophy in all sex/gender and age groups. The main questions it aims to answer are: 1. What's the patient journey of patients with Facioscapulohumeral Muscular Dystrophy? 2. How does Facioscapulohumeral Muscular Dystrophy burden the patients? 3. How's the quality of life of patients with Facioscapulohumeral Muscular Dystrophy? Patients with Facioscapulohumeral Muscular Dystrophy will be asked to: 1. fill a questionnaire. 2. be interviewed and answer questions about their illness experience, economic burden, quality of life and etc. Medical experts on Facioscapulohumeral Muscular Dystrophy will be asked to be interviewed and answer questions about understanding on the disease and the patients.

Participants needed: 300
Trial details
Biological sex: AllType: ObservationalSponsor: Xi'an Jiaotong UniversityUpdated: Jul 24, 2024Locations: 1
Eligibility criteria

Having been diagnosed as Facioscapulohumeral Muscular Dystrophy

No