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NCT06383247Recruiting

The Efficacy and Safety of Precision REpetitive Transcranial Magnetic Stimulation in Alleviating Motor Symptom in Parkinson's Disease

A Randomized, Double-blind, Multicenter, Placebo-controlled Trial (PRESS-PD)

Source: ClinicalTrials.gov · Last updated 17 Jun 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

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 symptoms of Parkinson's disease(PD) and delay the progression of the disease. In order to further explore the effectiveness of rTMS in the treatment of PD and lay the foundation for its clinical promotion, our research team plans to conduct a randomized double-blind controlled study of rTMS in the treatment of PD in multiple centers across the country.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
290 (estimated)
First submitted
22 Apr 2024
Start date
6 Dec 2024
Primary completion date
31 Dec 2026
Lead sponsor
Anhui Medical University
NCT number
NCT06383247

What you commit to

  • Study type: Interventional
  • Planned participants: 290
  • From 6 Dec 2024 to the primary completion date, 31 Dec 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Previously head MRI/CT was focal brain injury or severe leukoencephalopathy (Fazekas grade 3 and above);
  • Severe craniocerebral trauma, received craniocerebral surgery or deep brain stimulation treatment;
  • Participants in any clinical trial within the previous 6 month;

Other illness

  • Various secondary parkinsonism syndromes (vascular parkinsonism, Parkinsonism combined with parkinsonism, drug parkinsonism, etc.);
  • There are ferromagnetic implants in the body, such as cochlear implants, cardiac pacemakers, etc.
  • The person has 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;
  • Other conditions deemed unsuitable for inclusion by the investigator.

Other

  • Pregnant/lactating women or subjects (including men) who have a birth plan within 6 months;

Who the study is looking for

  • Age ≥ 40 years old;
  • Meet the diagnostic criteria for idiopathic Parkinson's disease (MDS Diagnostic Criteria for Parkinson's Disease (2015 Edition))\[1\];
  • Have no history of drug adjustment within 4 weeks before treatment and the entire study period;
  • The MDS-UPDRS Ⅲ score ≥8, and the Hoehn-Yahr rating is 1-4;
  • MMSE ≥22,able to cooperate with the completion of behavioral tests and transcranial magnetic stimulation therapy.

Age in the registry: 40 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Cognitive Neuropsychology Lab Anhui Medical University
Coordinator of this site? Confirm its status
HefeiChinaRecruiting

Related publications

This page is information, not medical advice. Discuss any trial with your doctor.