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Optimizing Door-to-reperfusion Times of One-stop Management in Acute Ischemic Stroke — ORETOM  

Acute Ischemic Stroke Clinical Trial

Official title:
Optimizing Door-to-reperfusion Times of One-stop Management in Acute Ischemic Stroke Trial

Clinical Trial Summary

Time is one of the most important in the decision of treatment of acute ischemic stroke. The optimal One-stop management from admission to recanalization associated with reduction of in-hospital times. The development of flat-detector computed tomography perfusion capable angio-suite allowed One-stop management to be improved treatment time better and better. To compare One-stop management versus our standard workflow in shortening door-to-recanalization time.

Clinical Trial Description

Acute ischemic stroke is one of the diseases associated with stroke onset time, especially in the case of large vessel occlusion within 6 hours. This is the reason why endovascular reperfusion therapy (mechanical thrombectomy, angioplasty, stent,…) is recommended to be performed as soon as possible in the comprehensive stroke centers. The successful recanalization within 6 hours demonstrated the efficacy that helps to improve the functional outcome by trials. Besides, the strategies shortening time from admission to successful recanalization are essential for the treatment of acute ischemic stroke due to large vessel occlusion. Nevertheless, the optimizing door-to-groin puncture and door to recanalization Time are the great challenge to benefit most patients with the endovascular therapy. In recent years, the One - stop management (direct transport to the angiosuite workflow) which means that the recanalization therapy is considered to perform immediately based on the diagnostic angiograms and perfusion maps relating to acute ischemic stroke caused by large vessel occlusion by the flat-detector computed tomography at the angiosuite at the same time. We hypothesized that one-stop management is feasible and reduces more intrahospital time delays than our standard workflow previously published. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05644938
Study type Interventional
Source Can Tho Stroke International Services Hospital
Contact
Status Enrolling by invitation
Phase N/A
Start date February 1, 2023
Completion date December 31, 2023
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