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- Withdrawn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
- Diseases
- Spinal muscular atrophy
- 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
Sites (6)
Sites in registry order. Save your city in your profile to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| CHU d Angers | Angers | France | Unknown status |
| CHU de Lille | Lille | France | Unknown status |
| CHU de Nantes | Nantes | France | Unknown status |
| Institute of Myology | Paris | France | Unknown status |
| CHU de Reims | Reims | France | Unknown status |
| CHRU de Tours | Tours | France | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.