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Identification of Biomarkers in Spinocerebellar Ataxia 3

Identification of Biomarkers in Spinocerebellar Ataxia 3

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03885167
Acronym
SCA3
Enrollment
22
Registered
2019-03-21
Start date
2019-02-21
Completion date
2023-01-04
Last updated
2023-11-22

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

Conditions

Spinocerebellar Ataxia Type 3

Brief summary

The purpose of this study is to examine the differences in cerebral spinal fluid (CSF) and blood of patients with spinocerebellar ataxias and healthy volunteers. The goal of this project is to identify new biomarkers that are useful for characterizing spinocerebellar ataxias and identify targets for treatment or prevention of this condition.

Detailed description

Participants will undergo a SARA exam, a lumbar puncture and a blood draw. A lumbar puncture is a procedure in which a small amount of the spinal fluid that surrounds the brain and spinal cord is removed by inserting a needle in the lower back. Participants will be asked not to eat or drink anything (water is acceptable) for at least 6 hours before the lumbar puncture visit. For this procedure, participants will be positioned lying on their side and curled up in a ball, or sitting up and bent forward, whichever is easier. Cushions will be used to enhance comfort. The lower back region will be cleaned and disinfected with an antiseptic iodine solution. The doctor will inject local anesthetic (lidocaine, 1%) into the skin of the lower back. This may produce a transient, mild burning sensation. A very small needle will be introduced into the skin and moved into fluid-filled space around the spinal nerves coming from the spinal cord. This may produce a pressure sensation. Approximately 2 tablespoons approximately 30 ml) of fluid will be collected. The needle will be removed and a band-aid applied over the needle insertion site. Participants will be asked to remain stationary, lying on flat for about ½ hour on a bed in the research clinic. Participants will be given something to eat and drink before leaving. Strenuous physical activity should be avoided for the next 24 hours. This includes lifting, bending, doing housework and gardening, or doing exercise such as jogging or bicycle riding. The SARA (Scale for the Assessment and Rating of Ataxia) exam is a clinical scale that assesses a range of different impairments in cerebellar ataxia. The scale is made up of 8 items related to gait, stance, sitting, speech, fingerchase test, nose-finger test, fast alternating movements and heel-shin test, and takes approximately 15 minutes to complete. The study also involves a single collection of about 3.5 tablespoons (approximately 50 ml) of blood. This blood draw may take place during a regularly scheduled visit to the neurology clinic or at the research appointment.

Interventions

OTHERSpecimen Collection

No interventions take place as part of study participation- only specimen collection occurs for both cohorts.

Sponsors

National Institutes of Health (NIH)
CollaboratorNIH
National Institute of Neurological Disorders and Stroke (NINDS)
CollaboratorNIH
University of Michigan
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

•Confirmed Genetic Testing of SCA3 or Healthy Volunteers

Exclusion criteria

* People with: * unstable thyroid * unstable intestinal/stomach issues * unstable heart issues * unstable liver issues * unstable kidney issues * unstable lung issues * unstable hormone issues * unstable mental disorders at screening * a tumor or evidence of having a tumor * a chronic infection or any severe acute infection within 3 months prior to screening * People who: * Take anti-coagulants and NSAIDs * Have started any investigational medications in the last month * Women who are pregnant or breast feeding

Design outcomes

Primary

MeasureTime frameDescription
Change in Ataxin 3 Levels in Cerebrospinal Fluid Specimens4 HoursA lumbar puncture is performed to collect CSF.
Change in Ataxin 3 Levels in Blood Plasma Specimens4 HoursA single blood draw is completed.

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026