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NCT05839145Withdrawn

Home Monitoring of Adult Patients With SMA: a Pilot Multicenter Validation Study

Source: ClinicalTrials.gov · Last updated 4 Nov 2026

Reason given: funding issues

Brief summary (registry, in English)

There is no complete cure for SMA yet. However, the discovery of the genetic cause of SMA has led to the development of several treatment options that affect the genes involved in SMA - a gene replacement therapy called Zolgensma, and two drugs, called Nusinersen (Spinraza) and Risdiplam (Evyrsdi). In this context, the evaluation of efficacy and the long term follow-up of patients treated with these innovative treatments in clinical routine is one of the critical points. These evaluations are carried out in a medical context (clinical sites or research unit) using validated measurement tools and outcome measures. Carrying out these evaluations in a controlled environment can be considered from certain aspects as an advantage (reproducibility of measures, neutral environment, etc.), but also raises a certain number of questions regarding the impact on patients, the financial cost, or the relevance of the data obtained in an unnatural environment (stress, fatigue, patient motivation…). Also the regulatory authorities ask for longitudinal data for deciding to reimburse these expensive treatments. As such, the hospital cannot digest all these evaluations due to a lack of resources.

Status (registry)
Withdrawn
Study type
Interventional
Enrollment
0 (actual)
First submitted
2 Dec 2022
Start date
6 Feb 2024
Primary completion date
1 Mar 2024
Lead sponsor
Institut de Myologie, France
NCT number
NCT05839145

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Any medical and social conditions that could interfere with the study under the appreciation of the medical coordinator

Other

  • Inability to comply with protocol requirements

Who the study is looking for

  • Age > 18 years
  • Confirmed SMA type 2 or 3 diagnostic
  • Written informed consent
  • Able to comply with all protocol requirements
  • Affiliate or beneficiary of a social security scheme
    • Non-Inclusion Criteria:
  • Inability to carry out assessments at home
  • Claustrophobia (only for patients from Paris and Lille sites)
  • Guardianship/trusteeship
  • Pregnant or nursing women

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (6)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
CHU d AngersAngersFranceUnknown status
CHU de LilleLilleFranceUnknown status
CHU de NantesNantesFranceUnknown status
Institute of MyologyParisFranceUnknown status
CHU de ReimsReimsFranceUnknown status
CHRU de ToursToursFranceUnknown status

Are you the coordinator? Confirm the details

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