NCT06919822Recruiting
SCAN Targeted Epidural Modulation for Parkinson's Disease
Somato-cognitive Action Network Targeted Epidural Modulation for Parkinson's Disease (STEM-PD): a Prospective Open-label Clinical Trial
Source: ClinicalTrials.gov · Last updated 19 Feb 2026
Brief summary (registry, in English)
The goal of this clinical trial is to learn if epidural modulation targeting the Somato-Cognitive Action Network (SCAN) can improve motor symptoms in adults with idiopathic Parkinson's disease (PD). It will also evaluate the safety of this treatment. The main questions it aims to answer are: * Does epidural modulation targeting SCAN reduce motor symptoms (measured by MDS-UPDRS-III scores) in PD patients after 3 months? * Is SCAN targeted epidural modulation (STEM) a safe and tolerable treatment for PD, with minimal adverse effects? Researchers will compare participants' baseline motor function to their post-treatment results to determine if STEM is effective. Participants will: * First undergo non-invasive brain stimulation (iTBS) to test responsiveness. * If eligible, receive surgical implantation of STEM electrodes in the personalized SCAN target. * Complete follow-up visits for 12 months to monitor symptoms, side effects, and quality of life.
- Status (registry)
- Recruiting
- Study type
- Interventional
- Enrollment
- 3 (estimated)
- First submitted
- 2 Apr 2025
- Start date
- 8 Dec 2025
- Primary completion date
- Sept 2026
- Lead sponsor
- Changping Laboratory
- Diseases
- Parkinson disease
- NCT number
- NCT06919822
What you commit to
- Study type: Interventional
- Planned participants: 3
- From 8 Dec 2025 to the primary completion date, Sept 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
- Presence of intracranial structural variants or other abnormalities that may interfere with TMS or surgical treatment, as detected by MRI or CT.
- Implantation of metallic medical devices such as deep brain stimulators, cochlear implants, vagus nerve stimulators, etc., which may affect MRI examination and TMS treatment.
- Contraindications to MRI scanning, including claustrophobia, tattoos, or magnetic metal-containing implants (to be confirmed with specialists).
- Receipt of other neuromodulation treatments (e.g., TMS, transcranial electrical stimulation, transcranial ultrasound stimulation) within the 1 months prior to enrollment.
Other illness
- Diagnosis of Parkinsonian superimposed syndrome or secondary Parkinson's disease.
- History of comorbid epilepsy or having first-degree relatives with a history of epilepsy.
- Contraindications to neurosurgery, such as bleeding or coagulation disorders.
- Presence of severe organic diseases, including heart failure, renal failure, or malignancies.
- Cognitive impairment as indicated by MMSE score of 24 or below.
- Significant speech impairment, hearing impairment, or visual impairment that limits cooperation with testing.
- Diagnosed psychiatric disorders based on DSM-V criteria or any psychological issues that may interfere with the study protocol.
- Active infections including hepatitis B virus (HBV), hepatitis C virus (HCV), syphilis, or human immunodeficiency virus (HIV) infection as determined by the investigator.
Age
- Women of childbearing age who are pregnant, breastfeeding, or intend to become pregnant during the trial.
Other
- Severe depression (HAMD-17 score of 24 or above) or severe anxiety (HAMA score of 29 or above).
- Alcohol or substance abuse.
- Any other medical abnormalities deemed by the investigator to be unsuitable for participation in the trial.
- Inability to complete follow-up visits due to geographical or other reasons.
- Participation in other clinical trials concurrently.
Who the study is looking for
- Diagnosed with idiopathic Parkinson's disease (PD) according to the revised clinical diagnostic criteria of the International Movement Disorder Society (MDS) (2015 version) or the Chinese Parkinson's Disease Diagnostic Criteria (2016 version).
- Age between 40 and 75 years, with a minimum age of 40 years at the time of diagnosis.
- Any gender, including both male and female patients.
- Hoehn-Yahr staging between 2 and 4 (inclusive).
- Disease duration of 5 years or more.
- Responding effectively to levodopa-based drug therapy with a minimum of 30% improvement in the levodopa loading test.
- Presence of motor fluctuations with or without anisocoria despite optimal drug treatment.
- Stable on medication for at least the past 1 month prior to screening and surgery.
- Ability to understand the trial and willingness to sign an informed consent form.
Age in the registry: 40 years to 75 years · Sex: All · Does not accept healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| The First Affiliated Hospital of Fujian Medical University Coordinator of this site? Confirm its status | Fuzhou | China | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.