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Repetitive Transcranial Magnetic Stimulation Therapy in Essential Tremor (rTMS)

S

Soochow University

Status

Enrolling

Conditions

Essential Tremor

Treatments

Device: real rTMS
Device: sham rTMS

Study type

Interventional

Funder types

Other

Identifiers

NCT06145932
JD-LK2023096-IR01

Details and patient eligibility

About

The purpose of this study is to evaluate the efficacy and electrophysiology of repetitive transcranial magnetic stimulation in the treatment of essential tremor.

Full description

This is a randomized controlled study.The purpose is to evaluate the efficacy of repetitive transcranial magnetic stimulation(rTMS) in the treatment of essential tremor,and explore the possible mechanism by detecting the changes of clinical scale and TMS-electroencephalogram(TMS-EEG), so as to seek an effective therapy for essential tremor.

Enrollment

40 estimated patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Diagnosed as essential tremor conforming to the diagnostic criteria for essential tremor in the tremor group of the International Parkinson's and Movement Disorders Society (IPMDS).
  2. Signed informed consent form.

Exclusion criteria

  1. Complicated with brain organic diseases, epilepsy, other mental diseases, family history of dementia, metal devices implanted in the body and any contraindications to TMS;
  2. History of craniocerebral surgery;
  3. TMS cannot cooperate;
  4. TMS-EEG examination artifacts are obvious, or cannot be analyzed due to other technical reasons.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

40 participants in 2 patient groups

rTMS treatment group
Experimental group
Description:
treated with real rTMS 1800 pulses / day,for 10 days
Treatment:
Device: real rTMS
Sham rTMS treatment group
Sham Comparator group
Description:
treated with sham rTMS 1800 pulses / day,for 10 days
Treatment:
Device: sham rTMS

Trial contacts and locations

1

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Central trial contact

Xiao-Yu Cheng, MD; Chun-Feng Liu, MD

Data sourced from clinicaltrials.gov

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