Muscle MRI Outlining of Neuromuscular Diseases Using Artificial Intelligence
NCT06917430 · Status: NOT_YET_RECRUITING · Type: OBSERVATIONAL · Enrollment: 120
Last updated 2025-04-08
Summary
Background and aim:
Neuromuscular diseases encompass a range of conditions affecting muscle cells, nerves, or the interaction between the two. A common pathological feature of these conditions is the pro-gressive replacement of muscle tissue with fat, which can be visualised using magnetic reso-nance imaging (MRI). MRI-based fat quantification serves as a key biomarker for disease characterisation, progression tracking, and treatment assessment. Currently, manual segmenta-tion of MRI scans for fat quantification is very time-consuming, requiring individual muscle delineation. Therefore, an artificial intelligence (AI) model is being developed to automate the segmentation. The aim of this study is to validate this AI model and assess its possibilities and limitations.
Method:
The study is ongoing. Retrospective MRI scans of patients with four different muscle diseases (anoctaminopathy, Becker muscular dystrophy, facioscapulohumeral muscular dystrophy, and hypokalemic periodic paralysis) are collected and manual delineation used for training the AI-model is being performed. The intramuscular fat fraction of individual muscles of the pelvis, thigh, and calf will be analysed using the AI model. The performance of the AI model will be compared to manual segmentation. The AI will be evaluated on metrics such as segmentation accuracy and time efficiency.
Conditions
- Becker Muscular Dystrophy
- FSHD - Facioscapulohumeral Muscular Dystrophy
- Hypokalemic Periodic Paralysis
Interventions
- OTHER
-
No intervention
No intervention.
Sponsors & Collaborators
-
Rigshospitalet, Denmark
lead OTHER
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2025-05-01
- Primary Completion
- 2035-01-01
- Completion
- 2035-01-01
More Related Trials
-
An MRI Study on Muscular Diseases -Pompe Disease and Dystrophia Myotonica-
NCT02708784 ·Status: UNKNOWN
-
Magnetic Resonance Imaging and Ultrasound Comparison With Load Evaluation
NCT06227182 ·Status: RECRUITING
-
1 Year MRI Followup in Facioscapulohumeral Muscular Dystrophy
NCT02159612 ·Status: COMPLETED
-
Magnetic Resonance Imaging (MRI) Muscle Phenotyping in Mitochondrial Disease
NCT02154711 ·Status: COMPLETED
-
Contractile Properties of Hypertrofic Muscles in Patients With Non-Dystrophic Myotonia
NCT04799366 ·Status: COMPLETED
-
Carbon-13 Magnetic Resonance Spectroscopy in Glycogen Storage Diseases
NCT04929002 ·Status: ACTIVE_NOT_RECRUITING
-
Critical Illness Myopathy as a Cause of Debilitating ICU-Acquired Weakness
NCT00937001 ·Status: ACTIVE_NOT_RECRUITING ·Phase: NA
-
New Imaging Biomarkers for Muscular Diseases - Multispectral Optoacoustic Imaging in Spinal Muscular Atrophy
NCT04115475 ·Status: COMPLETED ·Phase: NA
-
Nuclear Magnetic Spectroscopy Imaging to Evaluate Primary Lateral Sclerosis, Hereditary Spastic Paraplegia and Amyotrophic Lateral Sclerosis
NCT00023075 ·Status: COMPLETED
-
Reliability Study of a Motor Function Measure Digitalized Playful Completion Modules
NCT05227274 ·Status: COMPLETED
-
Ability of Muscle Imaging and Motor Function Measure (MFM) to Detect Changes in Disease Progression in Ambulant Spinal Muscular Atrophy Patients Compared to Healthy Volunteers.
NCT02044029 ·Status: COMPLETED
-
The Natural History and Muscle Fatigability of Patients With Congenital Myopathies.
NCT06157268 ·Status: RECRUITING
-
Serial Fasciculation Measurements in Motor Neurone Disease
NCT03809845 ·Status: COMPLETED ·Phase: NA
-
Diagnostic Evaluation of Patients With Neuromuscular Disease
NCT00015470 ·Status: COMPLETED
-
Contractile Cross Sectional Areas and Muscle Strength in Patients With Congenital Myopathies
NCT03018184 ·Status: COMPLETED
-
Aerobic Training in Patients With Congenital Myopathies
NCT02020187 ·Status: COMPLETED ·Phase: NA
-
Exploring the Physiologic, Pharmacodynamic, and Clinical Responses of Skeletal Muscle in Patients With Spinal Muscular Atrophy Treated With SMN-Directed Therapies
NCT06532474 ·Status: RECRUITING
-
Defining Endpoints in Becker Muscular Dystrophy
NCT05257473 ·Status: ACTIVE_NOT_RECRUITING
-
Research Biobank From Neuromuscular Biopsy Residues (in the Context of Care)
NCT06074822 ·Status: RECRUITING
-
Assessing Motor Neuron Disease Mechanisms by Threshold Tracking Transcranial Magnetic Stimulation and Magnetic Resonance Spectroscopy
NCT03664206 ·Status: WITHDRAWN
-
MYO-SHARE: MYO-MRI in Neuromuscular Diseases
NCT04866459 ·Status: ENROLLING_BY_INVITATION
-
Evaluation of Limb-Girdle Muscular Dystrophy
NCT00893334 ·Status: COMPLETED
-
Multispectral Optoacoustic Tomography for Advanced Imaging of Centronuclear Myopathy
NCT07021820 ·Status: RECRUITING
-
Study of Genotype and Phenotype Characterization in Duchenne Muscular Dystrophy With Small Mutations
NCT05833633 ·Status: UNKNOWN
-
Fat and Glucose Metabolism in Fed and Fasted State in Patients With Low Skeletal Muscle Mass
NCT03970135 ·Status: COMPLETED ·Phase: NA