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Clinical Trial Summary

Spinal muscular atrophy is a hereditary motorneuron disease caused by a mutation of the SMN1 gene, which is at the origin of a progressive limb and axial motor deficiency. It concerns 1200 individuals in France, including 700 adults in 2018. The main objective of this study is to assess the quality of life of SMA patients in France. The secondary objectives are, in one hand, to compare the quality of life of SMA patients to a population of neuromuscular diseases patients. And on the other hand to evaluate the determinants of participation and the impact of participation on quality of life in adult SMA patients.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05366465
Study type Observational
Source Hospices Civils de Lyon
Contact VUILLEROT Carole, Pr
Phone +334 72 12 95 04
Email carole.vuillerot@chu-lyon.fr
Status Recruiting
Phase
Start date October 19, 2022
Completion date October 19, 2024

See also
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