Effects of Transcranial Magnetic Stimulation After Endovascular Treatment for Acute Ischemic Stroke

Recruiting now · Not applicable · Has a placebo group

Conditions studied: Ischemic Stroke, Acute, Endovascular Thrombectomy

In brief

This is a multicenter, randomized, double-blind, sham-controlled trial, to determine the efficacy and safety of cTBS in treating patients with acute ischemic stroke after endovascular treatment.

Key facts

Study ID

NCT06639360

Run by

Xijing Hospital

People needed

60

Starts

2025-08-02

Expected to finish

2026-12-31

Last updated by the study team

2025-12-04

Who can join

Age: 18 and older, up to 80. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Patients with acute anterior circulation ischemic stroke aged between 18 and 80 years old.
• Imaging suggests that the infarction is caused by occlusion of the terminal portion of the internal carotid artery or the M1/M2 segment of the middle cerebral artery.
• A head CT within 24 hours of onset indicates an ASPECT score ≥6, and meets the guideline-recommended criteria for thrombectomy.
• Pre-stroke mRS score is ≤1.
• NIHSS score before thrombectomy is between 6 and 25.
• With vascular recanalization of mTICI > 2b/3.
• Informed consent form signed.

You may not qualify if…

• Patients with contraindications to TMS treatment, such as those with metallic foreign objects in the head, pacemakers, implantable drug pumps, cochlear implants, etc.;
• Patients with epilepsy, increased intracranial pressure, tumors, acute cerebral hemorrhage, or other severe neurological diseases, and those with severe functional impairment of organs such as the heart, liver, and kidneys;
• Head CT/MRI indicates midline shift or significant mass effect, or patients planned for surgical intervention;
• Head CT/MRI suggests acute cerebral infarction in both sides;
• Patients who are pregnant or breastfeeding;
• Patients with severe mental disorders or dementia who cannot cooperate with follow-up;
• Patients with other severe diseases resulting in an expected survival of less than 90 days;
• Patients who are participating in other interventional clinical studies within 30 days before the start of this study or after the onset of this condition;
• Patients who cannot cooperate with informed consent.

Where it is running

• Xijing Hospital — Xi'an, Shaanxi, China (enrolling)

Full record on ClinicalTrials.gov

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