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NCT04808388

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

Status unknown Last updated 16 September 2021
What this trial tests

trial testing MRI in Paramyotonia Congenita in 25 participants. Status unknown.

Timeline
2 February 2021
Primary endpoint
30 December 2021
31 December 2021

Quick facts

Lead sponsorRigshospitalet, Denmark
StatusStatus unknown
Study typeOBSERVATIONAL
Enrollment25
Start date2 February 2021
Primary completion30 December 2021
Estimated completion31 December 2021
Sites1 location across Denmark

Drugs / interventions tested

Conditions studied

Sponsor

Rigshospitalet, Denmark

Who can join

18 and older, any sex, with Paramyotonia Congenita or Nondystrophic Myotonia. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Muscle fat replacement and contractility in patients with skeletal muscle sodium channel disorders.
    Pedersen JJ, Stemmerik MG, Jacobsen LN, Skriver SV, et al · · 2023 · cited 7× · PMID 36782059 · DOI 10.1038/s41598-023-29759-7

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Other trials of MRI

Trials testing the same drug.

Other Rigshospitalet, Denmark trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04808388.

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