Status:

NOT_YET_RECRUITING

The Efficacy of Repetitive Transcranial Magnetic Stimulation in Parkinson's Disease:A Randomized, Double-blind, Multicenter, Placebo-controlled Trial

Lead Sponsor:

Anhui Medical University

Conditions:

Parkinson Disease

Transcranial Magenetic Stimualtion

Eligibility:

All Genders

40+ years

Phase:

NA

Brief Summary

Repetitive transcranial magnetic stimulation (rTMS) is a non-invasive and widely used neuromodulation technology. Small sample studies have shown that rTMS treatment can significantly improve the symp...

Detailed Description

As an innovative non-invasive neuromodulation technology, repetitive transcranial magnetic stimulation (rTMS) has demonstrated efficacy in improving motor symptoms in patients with Parkinson's disease...

Eligibility Criteria

Inclusion

  • Age ≥40 years old
  • Meet Movement Disorder Society standards;
  • Have no history of drug adjustment within 4 weeks before and during treatment;
  • The MDS-UPDRS Ⅲ score ≥8, and the Hoehn-Yahr rating is 1-4
  • MMSE ≥24,able to cooperate with the completion of behavioral tests and transcranial magnetic stimulation therapy.

Exclusion

  • Head MRI/CT ruled out focal brain injury or severe leukoencephalopathy (Fazekas grade 3);
  • Various secondary parkinsonism syndromes (vascular parkinsonism, Parkinsonism combined with parkinsonism, drug parkinsonism, etc.);
  • Severe craniocerebral trauma, received craniocerebral surgery or deep brain stimulation treatment;
  • There are ferromagnetic implants in the body, such as cochlear implants, cardiac pacemakers, etc.
  • The person or first-degree relatives have a history of epilepsy, unexplained loss of consciousness, or are taking anticonvulsant drugs to treat epileptic seizures;
  • Diagnosed with a neuropsychiatric disorder other than PD
  • Have a history of drug abuse or drug use;
  • Participants in any clinical trial within the previous 6 month;
  • Pregnant/lactating women or subjects (including men) who have a birth plan within 6 months;
  • Other conditions deemed unsuitable for inclusion by the investigator.

Key Trial Info

Start Date :

November 1 2024

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

June 30 2027

Estimated Enrollment :

312 Patients enrolled

Trial Details

Trial ID

NCT06583278

Start Date

November 1 2024

End Date

June 30 2027

Last Update

September 4 2024

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