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Clinical Trial Summary

This is a multicenter, sham-controlled, double-blind, randomized clinical trial to evaluate the efficacy and safety of lesion network mapping navigated cTBS in improving motor function in patients with acute ischemic stroke at 3-14 days after onset.


Clinical Trial Description

The target population of this study was patients with acute ischemic stroke. Lesion network mapping and navigation were used to select individual stimulation targets. Enrolled patients were randomly assigned in a 1:1 ratio to the "cTBS group" or the "Sham stimulation group" and received: cTBS group: Based on the map, an 8-shaped coil was used to stimulate the motor function-related targets. The stimulation intensity was RMT80%, 600 pulses, 50Hz, 40s per target, and the stimulation interval was more than 2 hours. The total course of treatment lasted 7 days. Sham stimulation group: A Sham stimulation coil was used to stimulate based on the map. The sound and duration were the same as the cTBS group, ensuring no effective stimulation. The total course of treatment lasted 7 days. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06400407
Study type Interventional
Source Beijing Tiantan Hospital
Contact Zixiao Li, MD
Phone +8613683234256
Email lizixiao2008@hotmail.com
Status Not yet recruiting
Phase Phase 2
Start date May 6, 2024
Completion date September 15, 2025