Clinical Trials Directory

Trials / Recruiting

RecruitingNCT06941961

iTBS for Acute Ischemic Stroke After Thrombectomy

Efficacy and Safety of Intermittent Theta Burst Stimulation in Acute Anterior Circulation Ischemic Stroke Patients Undergoing Mechanical Thrombectomy

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
178 (estimated)
Sponsor
Yi Yang · Academic / Other
Sex
All
Age
18 Years – 85 Years
Healthy volunteers
Not accepted

Summary

The goal of this randomized, single-blind, parallel-controlled clinical trial is to evaluate the efficacy and safety of intermittent theta burst stimulation (iTBS) as an adjunctive therapy for acute anterior circulation ischemic stroke patients who have undergone successful mechanical thrombectomy (MT). The study population includes adults aged 18-85 with NIHSS scores 5-25 post-MT and eTICI≥2b reperfusion.

Conditions

Interventions

TypeNameDescription
DEVICEintermittent theta burst stimulationThe iTBS delivered to the ipsilesional primary motor cortex (M1) at 80% resting motor threshold (RMT). Each session consists of 600 pulses (3-minute trains of 50 Hz triplets repeated every 10 seconds, twice daily with a 5-minute interval), administered for 7 consecutive days starting within 6 hours post-randomization.
DEVICEsham intermittent theta burst stimulationSham-iTBS is performed in the same way as the treatment group but uses 20% RMT.

Timeline

Start date
2025-04-25
Primary completion
2026-07-01
Completion
2026-08-01
First posted
2025-04-24
Last updated
2025-04-30

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT06941961. Inclusion in this directory is not an endorsement.