French Register of Patients With Spinal Muscular Atrophy

Phase

N/A

Condition

Myasthenia Gravis (Chronic Weakness)

Muscular Dystrophy

Spinal Muscular Atrophy

Treatment

N/A

Clinical Study ID

NCT04177134

APHP190245

N° IDRCB: 2019-A01161-56

All Genders

Study Summary

The primary objectives of the study are to obtain clinically meaningful data on survival and outcomes of all the patients with spinal muscular atrophy (SMA) 5q types 1 through 4 (according to international classification), being followed in the reference centers of the disease in France between September 1, 2016 and August 31, 2024. The registry will collect retrospectively and prospectively the longitudinal data of the long-term follow-up for child and adult patients, under real life conditions of current medical practice, in order to document the clinical evolution of patients (survival, motor, respiratory, orthopedic and nutritional), the conditions of use of the treatments, the mortality rates of treated and untreated patients, the tolerance of the treatments, adverse events in order to better define their places in the therapeutic strategy.

Eligibility Criteria

Inclusion

Inclusion Criteria:

Genetically confirmed SMA 5q patients through 1 to 4 types treated in referencecenters in France between September 1, 2016 and August 31, 2024.
for prospective study: inform consent form signed by patient.
for retrospective data: information form with non-opposition have been given toparticipant.
Covered by a health insurance.

Exclusion

Exclusion Criteria:

Other type of SMA (not 5q).
Under guardianship or curatorship.
Unable to understand french language.

Study Design

January 31, 2020

January 31, 2029

Study Description

As secondary objectives, the study aims:

to estimate the frequencies of patients with SMA 5q types 1 through 4 who have being treated in the reference centers between September 1 2016 and August 31 2024;
to describe overall demographic, familial, clinical, biological, and genetic characteristics of SMA 5q patients treated in all regions of France, by the type of SMA (type 1,2,3, and 4);
to study the impact of proactive and symptomatic medical interventions (bracing, IPPB devices) and medications (vaccinations, anti-infectious, digestive, nutritional supplements) in the evolution of patients;
to study the long-term evolution (survival, motor and respiratory functions, spinal shape, growth and nutritional function) of SMA 5q in treated and untreated populations, by new available therapies, throughout the register;
to study mortality rate of SMA 5q in treated and untreated populations, by new available therapies, throughout the register;
to identify and document the different therapeutic strategies by sub-populations and by discontinuation or follow-up of treatments;
to evaluate prognostic factors of responses to therapies;
to study the tolerance of treatments by type of treatments, by type of SMA and overall tolerance (including adverse events);
to estimate the costs of care for SMA 5q patients in different groups (types, ages);
to provide needful elements to evaluate the health care costs for the disease;
to study the autonomy and the quality of life of patients depending on different therapeutic strategies;
to study the impact of the disease on caregivers;
to facilitate development of scientific research on SMA in the conduct of trials on new therapeutic strategies.

Connect with a study center

Unité neuromusculaire, Service de Neurologie et Réanimation Pédiatrique, (French neuromuscular reference network (FILNEMUS), Hôpital Raymond Poincaré,
Garches, 92380
France
Active - Recruiting

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