Sign in

NCT06540417Completed

Study of the Effects of the Non-invasive Trigeminal Nerve Stimulation on Ischemic Stroke Patients

Study of the Neuroprotection and Rehabilitation Promotion of the Non-invasive Trigeminal Nerve Stimulation on Ischemic Stroke Patients

Source: ClinicalTrials.gov · Last updated 20 Jul 2025

Brief summary (registry, in English)

In patients with ischemic stroke, the primary focus revolves around enhancing the neuroprotective and rehabilitative effects of external trigeminal nerve stimulation (eTNS) and elucidating its underlying central mechanisms. Through clinical trials and neuroimaging studies, this research endeavors to 1) investigate the clinical impact of TNS on brain protection and 2) rehabilitation acceleration in ischemic stroke patients, while concurrently exploring the potential central nervous mechanisms involved. The ultimate aim is to contribute a novel therapeutic approach to the clinical management of acute ischemic stroke.

Status (registry)
Completed
Study type
Interventional
Enrollment
60 (actual)
First submitted
24 Jul 2024
Start date
25 Jul 2024
Primary completion date
1 Oct 2024
Lead sponsor
Xidian University
Diseases
Stroke
NCT number
NCT06540417

What you commit to

  • Study type: Interventional
  • Participants enrolled: 60
  • From 25 Jul 2024 to the primary completion date, 1 Oct 2024
  • 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

  • Current or recent participation in other neuromodulation stimulation therapies within the past 3 months;

Other illness

  • History of ischemic or hemorrhagic stroke within the past 3 months;
  • Any other life-threatening or severe medical condition that may interfere with the completion of the study protocol, including the 3-month follow-up;

Lab values

  • Severe allergic reaction to MR contrast agents or renal impairment, eGFR \<30 ml/min, excluding the use of contrast agents;

Other

  • Patients in a comatose state;
  • Pregnant or breastfeeding women;
  • Exclusion from trigeminal nerve stimulation: patients with trigeminal neuralgia or facial pain;
  • Refusal to sign the informed consent form;
  • Presence of contraindications related to MRI scanning.

Who the study is looking for

  • Age over 18 years;
  • Medically diagnosed with acute ischemic stroke;
  • Ability to receive trigeminal nerve stimulation within 72 hours post-stroke onset;
  • NIHSS (National Institutes of Health Stroke Scale) score ≥ 4;
  • Signed informed consent form;
  • Ability and willingness to comply with the study requirements.

Age in the registry: 18 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
Xidian University
Coordinator of this site? Confirm its status
Xi'anChinaUnknown status

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