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Clinical Trials in China / NCT06904716
Active, not recruiting Not applicable

The Study of Transcranial Magnetic Stimulation in the Regulation of Spinocerebellar Ataxia

NCT06904716 · tracked via the Priya Life Science China tracker
Sponsor
First Affiliated Hospital of Chongqing Medical University
Phase
Not applicable
Started
2023-05-01
Last updated
2025-04-01

Condition(s) studied

Spinocerebellar Ataxia

Investigational drug(s) / intervention(s)

Transcranial magnetic stimulation

Transcranial magnetic stimulation: Repetitive transcranial magnetic stimulation

Study summary

Spinocerebellar ataxia (SCA) is a group of hereditary neurological diseases caused by gene mutations leading to degenerative changes in the cerebellum, brainstem, and spinal cord. A key pathogenic mechanism of SCA is the repeated expansion of cytosine - adenine - guanine (CAG) trinucleotides in the coding region of specific genes. These repeated expansions are translated into abnormally large polyglutamine (PolyQ) tracts in proteins. These polyglutamine (PolyQ) tracts can cause changes in the excitability of the cerebral cortex in SCA patients. Quantitative electroencephalogram analysis (qEEG) is a modern type of electroencephalogram analysis that uses complex mathematical algorithms to process, transform, and analyze EEG signals, bringing new technologies for EEG signal feature extraction: specific frequency band and signal complexity analysis, connectivity analysis, and network analysis. It is sensitive to early neurodegenerative lesions. Using spectral analysis, nonlinear dynamics analysis, and functional connectivity analysis, we can explore the changes in cortical excitability and abnormal brain networks in SCA patients. Currently, the exploration of the quantitative electroencephalogram characteristics of SCA patients is still insufficient.

Eligibility

Sex
ALL
Min age
18 Years
Max age
75 Years
Healthy volunteers
Accepted
Inclusion Criteria: 1. Spinocerebellar ataxia patients confirmed through genetic testing 2. Patient aged 18-75 3. Patients who can walk independently (with the aid of a cane/walker) without assistance from others. 4. The SARA score exceeds 3. Exclusion Criteria: 1. Patients with unstable neurological disorders or accompanying medical conditions (such as stroke, arthritis, etc.) 2. Patients with significantly abnormal clinical indicators identified during screening 3. Patients concurrently participating in another clinical study 4. Patients with untreated intracranial hypertension, depression, dementia, or psychiatric disorders 5. Patients with severe heart disease 6. Patients who are wheelchair users 7. pregnant woman 8. Patients who cannot establish their identity or have limited legal capacity 9. Patients with contraindications for rTMS, including metallic objects in the head, history of neurosurgery, ferromagnetic bioimplants, metal coatings, history of seizures, autism, current use of protease inhibitors or other medications that may increase the risk of rTMS-induced seizures.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
the First Affiliatted Hospital of Chongqing medical Uiversity Chongqing Chongqing Municipality

More First Affiliated Hospital of Chongqing Medical University trials in China

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06904716 on ClinicalTrials.gov ↗ ← All trials in China