Characterization of the Clinical-epidemiological Profile of Patients With SMA5q Types II and III: Observational Study

  • STATUS
    Recruiting
  • participants needed
    100
  • sponsor
    Hospital Israelita Albert Einstein
Updated on 19 February 2024
atrophy
muscle atrophy
spinal muscular atrophy
nusinersen

Summary

This study aims to characterize the clinical-epidemiological profile and baseline characteristics of patients with spinal muscular atrophy (SMA) 5q types II and III in follow-up at the Brazilian Unified Public Health System (SUS). The study data will be based on patients medical records from several Brazilian public hospitals, which will be defined by the Brazilian Ministry of Health (MS).

Description

This is a retrospective cross-sectional observational study to characterize the clinical and epidemiological profile of patients with spinal muscular atrophy (SMA) 5q types II and III, in follow-up at the Brazilian Unified Public Health System (SUS). This study aims to provide baseline data, which in the future may be used by the Brazilian Ministry of Health (MS) to assess the effectiveness of nusinersen, as recommended in a risk sharing agreement established between MS and the pharmaceutical company that produces Spiranza (nusinersen). The clinical and epidemiological data will be collected from patients medical records, such as the score for the Hammersmith Functional Motor Scale - Expanded (HFMSE) and the Revised Upper Limb Module (RULM) at baseline, the WHO motor milestones at baseline, disease duration, age at the time of disease diagnosis, age at the time of disease screening, SMN2 (gene copy number), history of hospitalizations, history and characterization of previous surgical procedures, treatment dosage used, patient caregivers profile (ie, a family member or companion, who is responsible for taking care of the patient for most of the time). Other variables of interest that will also be collected are patients age and gender, geographic distribution, attending physician expertise and care structure where the patients were treated. The data acquisition will be performed using a paper and eletronic CRF (Case report Form). Written informed consent will be obtained from patients who meet the study elegibility criteria. The study will be performed in Brazilian public hospitals (centers) that are able to provide the treatment with nusinersen under the SUS scope. The total sample of patients and number of participating centers will be defined by the MS - SCTIE (Secretariat of Science, Technology and Strategic Supplies)/ DECIT (Department of Science and Technology). However, the initial estimation is a sample of 100 patients to be included in 10-15 centers.

Details
Condition Spinal Muscular Atrophy, Spinal Muscular Atrophy, Myelopathy, spinal cord disorders, spinal cord disorders
Age 1-100 years
Treatment Nusinersen Injectable Product
Clinical Study IdentifierNCT04404764
SponsorHospital Israelita Albert Einstein
Last Modified on19 February 2024

Eligibility

Yes No Not Sure

Inclusion Criteria

First-degree family member or companion responsible for taking care of the
patient with clinical diagnosis of SMA 5q type II or type III

Exclusion Criteria

Illiteracy
Refusal to participate in the study
Clear my responses

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