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A Registered Cohort Study on Spastic Paraplegia

A Registered Cohort Study on Spastic Paraplegia

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04006418
Enrollment
500
Registered
2019-07-05
Start date
2019-07-01
Completion date
2049-12-31
Last updated
2022-01-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Spastic Paraplegia

Brief summary

The aim of this study is to determine the clinical spectrum and natural progression of Hereditary Spastic Paraplegias(HSP) and related disorders in a prospective multicenter natural history study, to assess the clinical, genetic and epigenetic features of patients with Spastic Paraplegias to optimize clinicalmanagement..

Interventions

None listed

Sponsors

Wan-Jin Chen
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
OTHER

Eligibility

Sex/Gender
ALL
Healthy volunteers
Yes

Inclusion criteria

* Patients with the clinical diagnosis of spastic paraplegia * Clinical diagnosis of patients with spastic paraplegia * Unrelated healthy controls

Exclusion criteria

* Decline to participate. * There are serious interferences with individual participation and adherence to the research protocol, including but not limited to neurological, psychological, and/or medical conditions.

Design outcomes

Primary

MeasureTime frameDescription
Spastic Paraplegia Rating Scale (SPRS)6 monthsDisease severity will be assessed by application of the Spastic Paraplegia Rating Scale (SPRS), a clinical rating scale measuring disease severity in Hereditary Spastic Paraplegia (Schule et al. Neurology 2006). The SPRS contains 13 items, each ranging from 0 to 4 points. The total score is calculated as the sum of all items, yielding a range for the total score between 0 and 52. Hereby, higher SPRS total scores indicate more severe disease.

Countries

China

Contacts

Primary ContactYi Lin, MD,PhD
wanjinchen75@fjmu.edu.cn+13615039153
Backup ContactWan-Jin Chen, MD,PhD
wanjinchen75@fjmu.edu.cn+1386061359

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 21, 2026