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STOP-HSP.Net: a Registry for Hereditary Spastic Paraplegia as an Integration Tool for Future Therapeutic Strategies

Recruitingn/aAges any - anyAllIRCCS Fondazione Stella Maris
NCT06572046 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

Our goal is to create a solid and harmonious disease registry of patient affected by hereditary spastic paraplegia (HSP) that facilitates the collection and management of patients' data over time encouraging the research and the development of future clinical trials. In-depth clinical phenotyping will develop significant clinical outcome measures that can be used in clinical trials and will allow the phenotypic complexity of the disease to be captured with the use of validated clinical scales, biomarkers and so-called patient reported outcomes (PROs).

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📋 Eligibility rules (as published)
Inclusion Criteria: * clinical diagnosis of pure or complex HSP/spastic ataxia, even in the absence of a known genetic diagnosis * participants/parents/legal guardians will have to give informed consent for enrollment in the registry and privacy data management Exclusion Criteria: * subjects affected by secondary forms of HSP * presenting comorbidities that affect the general clinical picture according to clinical judgment * lack of informed consent
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What it tests

  • Not listed
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Where

1 site
IRCCS Fondazione Stella Maris
Pisa, Italy
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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