Sign in

NCT06665113Recruiting

Neuroprotective Effects of Long-term TaVNS in Early Parkinson's Disease Patients

A Double-blinded, Randomized, Parallel-group, Superiority Study to Explore the Neuroprotective Effects of Long-term Transcutaneous Auricular Vagus Nerve Stimulation(taVNS) in Early Parkinson's Disease(PD) Patients

Source: ClinicalTrials.gov · Last updated 14 Jan 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

This study is a randomized, double-blind, controlled trial exploring the effects of long-term taVNS intervention in patients with early-stage Parkinson's disease.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
12 (estimated)
First submitted
20 Oct 2024
Start date
23 Dec 2024
Primary completion date
Jun 2026
Lead sponsor
Kezhong Zhang
NCT number
NCT06665113

What you commit to

  • Study type: Interventional
  • Planned participants: 12
  • From 23 Dec 2024 to the primary completion date, Jun 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

  • Use of neuroprotective medications within 90 days prior to baseline, including monoamine oxidase B inhibitors (rasagiline, selegiline), certain dopamine receptor agonists (ropinirole), and GLP-1 receptor agonists such as Exenatide and NLY-01.
  • Use of any medications that may affect dopamine metabolism and/or dopamine receptors within 90 days prior to baseline, including typical and atypical antipsychotics, metoclopramide, α-methyl-dopa, flunarizine, apomorphine, amphetamine derivatives, bupropion, buprenorphine, cocaine, meperidine, methamphetamine, norephedrine, phentermine, modafinil, methylphenidate, procyclidine, reserpine, phenylpropanolamine, or MAO-A inhibitors.
  • Previous treatment with vagus nerve stimulation.
  • MRI contraindications (e.g., claustrophobia unresponsive to comfort or low-dose anxiolytics, dental implants) or MRI scans indicating clinically significant abnormalities in the brain, including but not limited to past hemorrhages or infarcts \> 1 cm³ or \> 3 lacunar infarcts.
  • Previous history of stroke or intracranial mass lesions.
  • Concurrent participation in other clinical trials.

Other illness

  • Patients with cognitive impairment (MMSE \< 24 and/or MoCA \< 26) or mental illnesses, or those unable to cooperate for other reasons.
  • Contraindications for taVNS, such as patients with cardiac pacemakers or a history of DBS surgery, or those planning surgery during the trial; ear conditions, such as tympanic membrane perforation.
  • Atypical or secondary Parkinsonian syndromes, including but not limited to those caused by trauma, brain tumors, infections, cerebrovascular diseases, or other neurological disorders, or symptoms confirmed by the investigator as drug, chemical, or toxin-related.
  • Patients with existing or potential cardiovascular diseases.
  • Ophthalmic diseases affecting eye movements.
  • Any neurological disorders other than Parkinsonian motor symptoms that interfere with gait or balance (e.g., chronic pain) or musculoskeletal injuries (e.g., fractures, stroke sequelae).
  • Severe organic diseases, such as late-stage tumors, with a life expectancy of less than 2 years.
  • Patients with a history of PD-related freezing episodes or falls.

Other

  • Inability to receive the required treatment and follow-up due to geographic reasons.
  • Any subject with an upper limb UPDRS tremor score of 3 or higher.

Who the study is looking for

  • Age 55-75 years.
  • Clinically diagnosed Idiopathic Parkinson's disease patients according to the 2016 Chinese diagnostic criteria for Parkinson's disease.
  • Hoehn and Yahr (H\&Y) stage ≤ 2.5 at medication initiation.
  • Parkinson's disease duration ≤ 3 years.
  • Receiving standard anti-Parkinson's disease medication treatment.

Age in the registry: 55 years to 75 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
The First Affiliated Hospital with Nanjing Medical University
Coordinator of this site? Confirm its status
NanjingChinaRecruiting

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