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Clinical Trials/NCT06064734
NCT06064734
Completed
Not Applicable

Low-Frequency REpetitive TRanscranial Magnetic Stimulation in ACute Ischemic StrokE Within 48 Hours (RETRACE-I): A Randomized, Open-label, Evaluator-blinded, Phase 2 Pilot Trial

Beijing Tiantan Hospital2 sites in 1 country60 target enrollmentMarch 11, 2024

Overview

Phase
Not Applicable
Intervention
LF-rTMS
Conditions
Stroke, Acute
Sponsor
Beijing Tiantan Hospital
Enrollment
60
Locations
2
Primary Endpoint
Proportion of Early neurological improvement (ENI)
Status
Completed
Last Updated
17 days ago

Overview

Brief Summary

This is a multicenter, open-label, evaluator-blinded, investigator-initiated, randomized clinical trial, to evaluate the clinical efficacy and safety of LF-rTMS in reducing infarct size, reducing disability rate and improving functional outcome in patients with acute ischemic stroke within 48 hours after stroke onset.

Detailed Description

The target population of this study was patients with clinically diagnosed AIS who had an acute occlusion of the responsible vessel in the anterior circulation and were not scheduled for intravenous thrombolysis and/or endovascular therapy, the time from stroke onset to the start of study intervention was less than 48-hours. Enrolled patients were randomly assigned in a 1:1 ratio to either the"LF-rTMS group" or the"Control group" to receive: 1. LF-rTMS group: H 4 Coil (stimulation site: prefrontal cortex, insular lobe),1-Hz rTMS, stimulation intensity RMT 100%,1200 pulses/session, two sessions (2400 pulses)/day (interval ≥2 hours), lasting about half an hour each time, the total duration of treatment was 3 days (6 sessions,7200 pulses). 2. Control group: received routine treatment. All the above therapeutic interventions were conducted by trained TMS operators. Except for the study intervention, the subjects in both groups received clinical routine diagnosis and treatment which were not affected by the intervention. All patients were followed up until the 90th day after randomization to evaluate the clinical efficacy and safety of LF-rTMS in reducing infarct size, reducing disability rate and improving functional outcome in patients with acute ischemic stroke within 48 hours after stroke onset.

Registry
clinicaltrials.gov
Start Date
March 11, 2024
End Date
October 25, 2025
Last Updated
17 days ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Beijing Tiantan Hospital
Responsible Party
Principal Investigator
Principal Investigator

Yongjun Wang

Professor

Beijing Tiantan Hospital

Eligibility Criteria

Inclusion Criteria

  • Age 18-80 years, gender is not limited;
  • Acute ischemic stroke of anterior circulation was diagnosed clinically
  • mRS 0-1 score before onset;
  • 6 ≤ NIHSS ≤25 at randomization;
  • Within 48 hours of stroke onset;
  • No thrombolysis therapy or thrombectomy is planned;
  • Obtain informed consent signed by the patient himself or by his legal authorized representative.

Exclusion Criteria

  • TMS contraindications include metallic foreign bodies in the head, pacemaker, implantable drug pumps, cochlear implants, etc.
  • Epilepsy or history of epilepsy, intracranial hypertension, tumor and other serious neurological disorders;
  • Midline displacement and brain parenchymal mass effect seen in head CT and other images;
  • Head CT or MRI showed bilateral acute cerebral infarction, brainstem infarction, or insular infarction;
  • Evidence of acute intracranial hemorrhage;
  • A history of congenital or acquired hemorrhagic disease, coagulation factor deficiency, or thrombocytopenia disease;
  • After blood pressure control, the systolic blood pressure was still ≥180 mmHg or the diastolic blood pressure was ≥110 mmHg;
  • Known recent or current serum creatinine exceeding 1.5 times the upper limit of normal or estimated glomerular filtration rate (EGFR) \< 60 mL/min;
  • Patients during pregnancy or lactation and within 90 days of planned pregnancy;
  • Patients with severe mental disorders or dementia who can not cooperate with informed consent and follow-up;

Arms & Interventions

LF-rTMS

H 4 Coil (stimulation site: prefrontal cortex, insular lobe),1-Hz rTMS, stimulation intensity RMT 100%,1200 pulses/session, two sessions (2400 pulses)/day (interval ≥2 hours), lasting about half an hour each time, the total duration of treatment was 3 days (6 sessions,7200 pulses).

Intervention: LF-rTMS

Control

Routine treatment.

Outcomes

Primary Outcomes

Proportion of Early neurological improvement (ENI)

Time Frame: 3 days

Proportion of patients with a reduction of ≥4 on the NIHSS, compared with the baseline score or an NIHSS of 0 or 1

Infarct growth

Time Frame: 3 days

Infarct growth at 3 days was calculated as the absolute difference between the baseline core infarct volume and the 3 days post-randomization infarct volume.

Symptomatic intracranial hemorrhage

Time Frame: 3 days

The proportion of symptomatic intracranial hemorrhage

Infarct growth from baseline to Day 3 (mL)

Time Frame: 3 days

Infarct growth at 3 days was calculated as the absolute difference between the baseline core infarct volume and the 3 days post-randomization infarct volume. Positive values indicate infarct growth.

Secondary Outcomes

  • mRS scores of 0-1(90 days)
  • Final infarct volume(3 days)
  • mRS scores of 0-2(90 days)
  • Barthel index of ADL(90 days)
  • Montreal Cognitive Assessment (MoCA) total score(90 days)
  • All-cause deaths(90 days)
  • Stroke recurrence(90 days)
  • △NIHSS score(3 days)
  • Serious adverse events(90 days)
  • Symptomatic intracranial hemorrhage(90 days)
  • Deterioration of neurological function(3 days)
  • Adverse events (AE)(90 days)
  • EQ-5D-5L(90 days)
  • Proportion of Early neurological improvement (ENI)(3 days)
  • Final infarct volume at Day 3 (mL)(3 days)
  • Change in NIHSS score from baseline to Day 3(3 days)
  • Proportion of participants with modified Rankin Scale score 0 to 1 at Day 90(90 days)
  • Proportion of participants with modified Rankin Scale score 0 to 2 at Day 90(90 days)
  • Number of participants with neurological deterioration within 3 days(3 days)
  • Number of participants with symptomatic intracranial hemorrhage within 90 days(90 days)

Study Sites (2)

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