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NCT06630702Recruiting

Application of Thoracic Epidural SCS for Managing FOG in Patients With Advanced Parkinson's Disease

Application of Thoracic Epidural Spinal Cord Stimulation (SCS) for Managing Freezing of Gait (FOG) in Patients With Advanced Parkinson's Disease

Source: ClinicalTrials.gov · Last updated 20 Nov 2025

Brief summary (registry, in English)

Spinal cord stimulation (SCS) has proven to be effective for pain that is unresponsive to medication. This technique involves an anesthesiologist or a neurosurgeon placing stimulation electrodes at the thoracic vertebrae to provide pain relief. Although SCS is not currently a standard treatment for patients with Parkinson's disease, recent studies have shown that Parkinson's patients who experience intolerable pain and undergo SCS treatment not only experience pain relief but also show improvements in gait and other Parkinson's symptoms. Therefore, the investigators aim to use temporary, minimally invasive SCS electrodes to help patients with nrFOG (non-responsive Freezing of Gait) improve their stability and reduce their risk of falls.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
5 (estimated)
First submitted
18 Sept 2024
Start date
20 Sept 2024
Primary completion date
31 Dec 2027
Lead sponsor
National Taiwan University Hospital
NCT number
NCT06630702

What you commit to

  • Study type: Interventional
  • Planned participants: 5
  • From 20 Sept 2024 to the primary completion date, 31 Dec 2027
  • 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

  • Medication-controlled frozen gait.
  • It is expected that the implantation area has undergone previous surgery or there is infection near the implantation area, which may affect the success rate of implantation or increase concerns about complications (such as severe extraspinal adhesion, or spinal cord damage in previous surgeries).
  • People with abnormal coagulation function (such as hemophilia patients) or those who have been controlled by long-term use of antithrombotic drugs and cannot stop taking them in a short period of time.

Other illness

  • Atypical Parkinson's disease.
  • CDR (Clinical Dementia Rating Scale) ≧2. 8. Those who are allergic to developer.

Other

  • Patients with spinal cord injuries.
  • It is expected that there are lesions near the implantation area causing spinal canal stenosis or myelopathy (can be ruled out by MRI).

Who the study is looking for

  • Age:40-85 years old.
  • Patients with primary Parkinson\'s disease who have been diagnosed by a movement disorder specialist for more than 5 years. Although they have a clear response to drugs, they have a frozen gait that cannot be controlled by drugs. Lower limb pain may be present with or without Parkinson\'s non-motor symptoms.
  • No other secondary gait problems.

Age in the registry: 40 years to 85 years · 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
National Taiwan University Hospital Hsin Chu Branch
Coordinator of this site? Confirm its status
HsinchuTaiwanRecruiting

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