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UnknownNCT04808388

Using MRI in Patients With Non-dystrophic Myotonia to Access Muscle Contractility

Using MRI to Quantify Fatty Infiltration in Muscle Tissue, and Compare it to Isometric Muscle Strength Measurements and (2) Use Questionnaires, Systemic Interview and Simple Myotonic Bed-side Tests to Describe the Phenotype.

Status
Unknown
Phase
Study type
Observational
Enrollment
25 (estimated)
Sponsor
Rigshospitalet, Denmark · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

The aim of this project is (1) to investigate whether or not structural muscle abnormalities could be a consequence of the disorder and (2) to provide further clinical description of this rare phenotype. To do so, the investigators will (1) use Dixon MRI to quantify fatty infiltration in muscle tissue and compare it to muscle strength measurements from isometric dynamometry in order to access contractility and (2) describe the myotonic phenotype with simple squeeze test and questionnaires.

Detailed description

Non-dystrophic myotonias are rare genetic diseases in which the membrane excitability is altered by mutations in genes encoding muscle ion channels. Patients suffer from myotonic stiffness, pain, fatigue and sometimes paralysis. Non-dystrophic myotonia is distinct from myotonic dystrophies with the absence of muscle degeneration. Paramyotonica congenita is characterzied by paradoxial myotonia, which, in contrast to the more common myotonia congenita, is myotonic stiffness that worsens with activity. Typically, the first few contractions seem normal, whereas repetition leads to severe stiffness. Our hypophysis is that these patient might also suffer from muscle degeneration.

Conditions

Interventions

TypeNameDescription
OTHERMRIUsing MRI for fat fraction and Biodex for isometric strength

Timeline

Start date
2021-02-02
Primary completion
2021-12-30
Completion
2021-12-31
First posted
2021-03-22
Last updated
2021-09-16

Locations

1 site across 1 country: Denmark

Source: ClinicalTrials.gov record NCT04808388. Inclusion in this directory is not an endorsement.