Skip to main content
OpenTrials
Completed

NCT Number: NCT01611610

Clinical Assessment of Spinal Muscular Atrophy Type II and III (SMA Europe)

The aim of this project is to establish a network of clinical teams including the major neuromuscular centers in Europe.

We plan to work together to find the best common outcome measures for the following multicenter therapeutic trials.

Completed

Looking for future studies?

Notify Me

Key information

About this study

16 patients (6 ambulant and 10 non ambulant), affected by type II and type III SMA will be enrolled and assessed at baseline and 6 and 12 months later. Non ambulant patients will be assessed using the modified version of the Hammersmith Motor Functional Scale while ambulant patients will be assessed using the extended module of the Hammersmith Motor Functional Scale and timed items, the 6 minute walk and a step activity monitor. All patients will also be assessed using the Motor Function Measure (MFM), that covers the whole range of activities for both ambulant and non ambulant patients. All measures will undergo a process of validation including inter observer reliability. This information will be most valuable for any future trial and will make the groups involved ready to participate to future collaborative studies saving a lot of time on the preliminary aspects (validation, reliability, training) that will be fulfilled by the present study. The study will also provide natural history data for a 12 month period on patients with SMA II and III.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

for ambulant patients:

  • age between 30 months and 24 years
  • documented SMA diagnosis by genetic tests; Each should also have the determination of the SMN2 copy number
  • able to walk 10 meters without support
  • subject who signed an informed consent- subject affiliated to a social security system

Inclusion criteria

non ambulant patients:

  • documented diagnosis of SMA by genetic tests
  • not able to walk 10 meters without support
  • subject affiliated to a social security system
  • subject who signed an informed consent

Exclusion criteria

  • Patient who are currently involved in other clinical trials
  • severe intellectual impairment limiting the comprehension of the demanded tasks
  • acute neurologic, inflammatory, infectious, endocrine, orthopedic disease in the month preceding the inclusion
  • chronic neurologic (besides SMA), inflammatory, infectious, endocrine, orthopedic disease which are not a natural consequence of SMA
  • spinal surgery scheduled 6 months before or within 12 months after enrollment
  • pregnant women

Treatment and study plan

functional tests

Other

The ambulant patients will perform

  • MFM (20 items)
  • Hammersmith modified module - MHMFS
  • Timed tests (time to rise from the floor,...)
  • 6 minute walk test
  • PedsQL - neuromuscular module

Primary outcomes

  1. Change from baseline in total score of Motor Function Measure at one year

    Time frame: at baseline and one year after

Secondary outcomes

  1. Change from baseline of Pediatric Quality of Life Inventory Score at one year

    Time frame: at baseline and one year after

    Pediatric Quality of Life Inventory - neuromuscular module

Sponsors and collaborators

Lead sponsor

Institut de Myologie, France

Other

Registry information

Official study title

Clinical Assessment of Spinal Muscular Atrophy Type II and III

Important dates

Study start
2011
Primary completion
2013
Study completion
2013
First posted
Jun 5, 2012
Registry last updated
Mar 5, 2014

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.