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NCT04656210Active, not recruiting

Myotonic Dystrophy - Vascular and Cognition

Links Between Diabetes and Cognitive Impairment in Myotonic Dystrophy Type 1 : a Non-conventional MRI Study

Source: ClinicalTrials.gov · Last updated 22 May 2026

Brief summary (registry, in English)

The cognitive disorders of adult forms of myotonic dystrophies type 1 are heterogeneous (impairment of executive functions, visio construction and theory of the mind, which can progress to the stage of dementia). Nevertheless, patients have very different degrees of cognitive impairment. Expansion of CTG triplets disrupts the alternative splicing of mRNAs of various proteins, including the insulin receptor and Tau protein. Type 2 diabetes, associated with peripheral insulin resistance, is therefore common in this pathology. Type 2 diabetes,could to explain the cognitive impairment of patients, through the accelerated development of brain lesions (especially tauopathy and cerebral atrophy).

Status (registry)
Active, not recruiting
Study type
Observational
Enrollment
85 (actual)
First submitted
23 Nov 2020
Start date
14 Oct 2021
Primary completion date
13 Oct 2024
Lead sponsor
University Hospital, Lille
NCT number
NCT04656210

What you commit to

  • Study type: Observational
  • Participants enrolled: 85
  • From 14 Oct 2021 to the primary completion date, 13 Oct 2024
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Neurological history other than neuropathy: epilepsy, stroke, dementia
  • Major comorbidity considered as a contraindication by the investigator (cancer, unstable angina, etc.).

Age

  • Pregnancy or breastfeeding or woman of childbearing age without effective contraception (a pregnancy test will be done)
  • Persons of full age deprived of their liberties by a judicial or administrative decision

Other

  • Contra indication to MRI
  • Person under guardianship or curators

Who the study is looking for

  • Molecularly proven type 1 myotonic dystrophy
  • Voluntary, having given informed consent
  • Socially insured patient
  • Patient willing to comply with all study procedures and duration (3 hours + MRI 35 minutes)
  • Patient insured under the French social security system
  • Signed consent form

Age in the registry: 18 years to 75 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Hopital Roger Salengro, CHU Lille
Coordinator of this site? Confirm its status
LilleFranceUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.