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The Influence of Deep TMS on Cerebellar Signs in Patients With Machado Joseph Disease

The Influence of Deep Repetitive Transcranial Magnetic Stimulation (TMS) on Cerebellar Signs in Patients With Spinocerebellar Ataxia Type 3 (SCA3 - Machado Joseph Disease)

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02039206
Enrollment
20
Registered
2014-01-17
Start date
2014-02-28
Completion date
2016-06-30
Last updated
2018-01-25

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

Conditions

Machado Joseph Disease (SCA3)

Keywords

Machado Joseph disease, Deep TMS, TMS, Transcranial Magnetic Stimulation, SCA3, Magnetic Stimulation, Brainsway

Brief summary

To test the effects of low frequency deep rTMS using the novel HCERMJD-coil on cerebellar deficits in patients with SCA3 and to establish its safety in this population. Investigator is anticipate that stimulation of the cerebellum with the novel HCERMJD-coil may induce significantly therapeutic effects in patients with SCA3 and will pave the way for establishing a novel and effective treatment for this disorder.

Interventions

DEVICEDeep TMS

1Hz Stimulation

Sponsors

Brainsway
Lead SponsorINDUSTRY

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
20 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* SCA3 patients aged 20 - 80 years, with detectable clinical signs and confirmed genetic diagnosis.

Exclusion criteria

1. Patients who have concomitant epilepsy. 2. History of seizure or heat convulsion. 3. Patients on neuroleptics. 4. Patients with dementia (MMSE\<25) or any unstable medical disorder. 5. History or current unstable hypertension. 6. History of head injury or neurosurgical interventions. 7. History of any metal in the head (outside the mouth). 8. Known history of any metallic particles in the eye, implanted cardiac pacemaker, implanted neurostimulators, surgical clips (above the shoulder line) or any medical pumps. 9. History of frequent or severe headaches. 10. History of migraine. 11. History of hearing loss. 12. History of cochlear implants 13. History of drug abuse or alcoholism. 14. Pregnancy or not using a reliable method of birth control. 15. Participation in current clinical study or clinical study within 30 days prior to this study.

Design outcomes

Primary

MeasureTime frame
Scale for the Assessment and Rating of Ataxia (SARA)30 days

Countries

Israel

Outcome results

None listed

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