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NCT04602195Completed

Responsiveness and Validation Study of MFM-32 in SMA Patients Treated With Nusinersen

Responsiveness and Validation Study of MFM-32 in SMA Patients Treated With Nusinersen: NusiMFM

Source: ClinicalTrials.gov · Last updated 21 Dec 2023

Brief summary (registry, in English)

The Motor Function Measure (MFM), a reliable tool assessing motor function and its progression in most neuromuscular diseases, is widely used in France in many teams. It can be used regardless of the severity of the motor impairment or the ambulatory status of the patient, allowing its use throughout the whole follow-up period of the patient, even in case of the loss of walking. Two versions of the MFM exist, one composed of 32 items originally validated for patients from 6 years old (MFM-32) and a shorter version composed of 20 items originally validated for patients between 2 and 6 years old (MFM-20). In order to prove the possible use of MFM-32 as early as the age of 2 years to validly and reliably monitor the evolution of the motor function of children treated with Nusinersen, we propose in this project to study the sensitivity to treatment-induced change of MFM-32 and the validity of the scale in this population.

Status (registry)
Completed
Study type
Observational
Enrollment
33 (actual)
First submitted
20 Oct 2020
Start date
19 Jan 2021
Primary completion date
10 Nov 2023
Lead sponsor
Hospices Civils de Lyon
NCT number
NCT04602195

What you commit to

  • Study type: Observational
  • Participants enrolled: 33
  • From 19 Jan 2021 to the primary completion date, 10 Nov 2023
  • 10 sites 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

  • Patients with associated cognitive impairment making impossible evaluation of motor function

Other

  • Patients participating to a clinical study with a potential effect on their motor function.

Who the study is looking for

  • Boys and girls with Type 1 or 2 Spinal Muscular Atrophy, genetically confirmed
  • Aged 2 to 6 years old
  • Treated by Nusinersen for at least two months
  • With parental assent

Age in the registry: 2 years to 6 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (10)

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

SiteCityCountrySite status
Service de neuropédiatrie et neurochirurgie de l'enfant Centre de Référence des Maladies Neuromusculaires AOC CHU d'Angers
Coordinator of this site? Confirm its status
AngersFranceUnknown status
Centre de Référence des maladies neuromusculaires Centre Hospitalier Régional Universitaire de Brest
Coordinator of this site? Confirm its status
BrestFranceUnknown status
L'Escale, Service central de rééducation pédiatrique Hospices Civils de Lyon Hôpital Mere Enfant
Coordinator of this site? Confirm its status
BronFranceUnknown status
Service de génétique médicale Pôle de Pédiatrie CHU Estaing
Coordinator of this site? Confirm its status
Clermont-FerrandFranceUnknown status
Service de Neurologie et réanimation pédiatriques
Coordinator of this site? Confirm its status
GarchesFranceUnknown status
Apf Esean
Coordinator of this site? Confirm its status
NantesFranceUnknown status
Institut I-Motion - Centre de recherche pédiatrique en pathologies neuromusculaires
Coordinator of this site? Confirm its status
ParisFranceUnknown status
Service de pédiatrie CHU de Saint-Etienne
Coordinator of this site? Confirm its status
Saint-Priest-en-JarezFranceUnknown status
Service de Neuropédiatrie CHU de Strasbourg - Hôpital de Hautepierre
Coordinator of this site? Confirm its status
StrasbourgFranceUnknown status
Unité de Neurologie Pédiatrique Centre de Référence Maladies NeuroMusculaires Hôpital des Enfants CHU Toulouse
Coordinator of this site? Confirm its status
ToulouseFranceUnknown status

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