Advancing Reperfusion Therapy for Ischemic Stroke: Direct Transfer to Angiography Suite for Patie⦠(NCT07460713) | Clinical Trial Compass
Not Yet RecruitingNot Applicable
Advancing Reperfusion Therapy for Ischemic Stroke: Direct Transfer to Angiography Suite for Patients With Suspected Large Vessel Occlusion
China568 participantsStarted 2026-03-31
Plain-language summary
The investigators initiated a multicenter, prospective, randomized, open-label, blinded-endpoint (PROBE) controlled trial to evaluate the efficacy and safety of the direct transfer to angiography suite (DTAS) triage strategy compared to the conventional triage strategy with CT/MRI in patients with suspected large artery occlusive (LVO) within 6 hours of symptom onset.
Who can participate
Age range18 Years
SexALL
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Ageā„18 years old;
* Patients presenting with symptoms or signs suggestive of acute large vessel occlusion (LVO) strokeļ¼
* Randomization within 6 hours of symptom onsetļ¼
* Baseline NIHSS score ā„10 points prior to randomization;
* Pre-stroke modified Rankin Scale (mRS) score ā¤2;
* Written informed consent from patients or their legally authorized representatives.
Exclusion Criteria:
* Refusal of endovascular treatmentļ¼
* Allergy to contrast agents;
* Clinical symptoms or signs suggestive of intracranial hemorrhage (e.g., severe headache, seizures, or signs of increased intracranial pressure);
* Transferred patients (e.g., from centers without thrombectomy capability);
* Seizure at stroke onset, postictal paralysis, or inability or unwillingness to cooperate due to epilepsy or other neurological or psychiatric disorders;
* Clinically unstable conditions requiring urgent life-support treatment;
* Other standard contraindications to endovascular treatment;
* Any terminal illness such that the patient would not be expected to survive more than 1 year;
* Pregnant women, nursing mothers, or women with a positive pregnancy test at admission;
* Unlikely to adhere to the trial protocol or follow-up;
* Any condition that, in the judgment of the investigator could impose hazards to the patient if study therapy is initiated or affect the participation of the patient in the study;
* Participation in other interventional clinical trials within the previous 3 months.
What they're measuring
1
The modified Rankin Scale (mRS) score 0-2 at 90 days