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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03204773
Other study ID # NMS in HSP
Secondary ID
Status Completed
Phase
First received
Last updated
Start date April 28, 2018
Est. completion date July 30, 2019

Study information

Verified date August 2020
Source University Hospital Tuebingen
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Comparing the non-motor symptoms of patients with hereditary spastic paraplegia (HSP) to healthy controls (spouses, relatives or other healthy controls) by using the a number of specific questionaires


Description:

https://lamapoll.de/NMS_in_HSP


Recruitment information / eligibility

Status Completed
Enrollment 236
Est. completion date July 30, 2019
Est. primary completion date July 1, 2019
Accepts healthy volunteers
Gender All
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria:

- Group 1: Patients with HSP (hereditary spastic paraplegia)

- Group 2: Healthy controls

- Age 18 to 70 years

- Written, informed consent

Exclusion Criteria:

- Lack of ability for a written, informed consent

- Presence of spastic gait disorder or other neurological condition (Group 2)

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
EuroQol five dimensions questionaire (EQ-5D)
Testing quality of life.
Modified Fatigue Impact Scale (MFI)
Screening for fatigue
Brief Pain Inventory (BPI)
Testing for pain
Becks Depression Inventory (BDI)
Screening for depression
Restless-leg Questionaire (RLS diagnostic criteria)
Testing for restless-legs

Locations

Country Name City State
Germany University Hospital Tübingen, Center for Neurology Tübingen

Sponsors (1)

Lead Sponsor Collaborator
University Hospital Tuebingen

Country where clinical trial is conducted

Germany, 

References & Publications (1)

Rattay TW, Boldt A, Völker M, Wiethoff S, Hengel H, Schüle R, Schöls L. Non-motor symptoms are relevant and possibly treatable in hereditary spastic paraplegia type 4 (SPG4). J Neurol. 2020 Feb;267(2):369-379. doi: 10.1007/s00415-019-09573-w. Epub 2019 Oc — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Identification of relevant non-motor symptoms in SPG4 By using the five mentioned scales we try to identify relevant non-motor symptoms day 1
See also
  Status Clinical Trial Phase
Recruiting NCT04712812 - Registry and Natural History Study for Early Onset Hereditary Spastic Paraplegia

External Links