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
| Type | Name | Description |
|---|---|---|
| DEVICE | intermittent theta burst stimulation | The 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. |
| DEVICE | sham intermittent theta burst stimulation | Sham-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.