RECRUITINGOBSERVATIONAL
STOP-HSP.Net: a Registry for Hereditary Spastic Paraplegia as an Integration Tool for Future Therapeutic Strategies
About This Trial
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).
Who May Be Eligible (Plain English)
Who May Qualify:
- 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 willing to sign a consent form for enrollment in the registry and privacy data management
Who Should NOT Join This Trial:
- subjects affected by secondary forms of HSP
- presenting comorbidities that affect the general clinical picture according to clinical judgment
- lack of willing to sign a consent form
Always talk to your doctor about whether this trial is right for you.
Original Eligibility Criteria
View original clinical language
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
Locations (1)
IRCCS Fondazione Stella Maris
Pisa, Italy