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A study of the efficacy and safety of repetitive transcranial magnetic stimulation in patients with spinocerebellar ataxia

A study of the efficacy and safety of repetitive transcranial magnetic stimulation in patients with spinocerebellar ataxia

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100046902
Enrollment
Unknown
Registered
2021-05-30
Start date
2019-10-01
Completion date
Unknown
Last updated
2022-01-10

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

Conditions

spinocerebellar ataxia

Interventions

experimental group 1:1 Hz rTMS
experimental group 2:iTBS

Sponsors

Xiangya Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Diagnosis as spinocerebellar ataxia type 1 or 2 or 3 by genetic testing; 2. Age between 18 to 65 years, man or woman; 3. Scale of gait from 2 to 6 in Scale for the Assessment and Rating of Ataxia (SARA); 4. Patients with no drug therapy or stable drug therapy within 1 month before screening; 5. Subjects who never receive rTMS or stem cell therapy within 3 months before screening; 6. Not paticipating in other clinical trials during study; 7. Consent informed before study.

Exclusion criteria

Exclusion criteria: Exclusion criteria for rTMS therapy: 1. Patients with other neurological and psychiatric diseases; 2. Patients with diseases that disturb scale grading, e.g. fracture failure; 3. Pregnant or breast-feeding women; 4. Patients with intracranial or intracardiac implants, e.g. deep brain stimulator, cardiac pacemaker. Exclusion criteria for MRI examination: 1. Patients with other chronic somatic diseases, e.g. hypertension, diabetes; 2. Patients with intracranial or intracardiac implants, e.g. deep brain stimulator, cardiac pacemaker; 3. Patients with helicobia; 4. Patients take neurological and psychiatric drugs, e.g. sedative-hypnotics, antiepileptic drugs, antipsychotic drugs, or narcotics.

Design outcomes

Primary

MeasureTime frame
Scale for the Assessment and Rating of Ataxia;International Cooperative Ataxia Rating Scale;magnetic resonance spectroscopy;resting-state functional magnetic resonance imaging;

Secondary

MeasureTime frame
Ten Miles Walk Test;9-Hole Peg Test;PATA test;

Countries

China

Contacts

Public ContactJiang Hong

Xiangya Hospital

jianghong73868@126.com+86 13975806840

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026