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WE-TRUST (Workflow Optimization to Reduce Time to Endovascular Reperfusion for Ultra-fast Stroke Treatment)

Stroke, Acute Clinical Trial

Official title:
WE-TRUST (Workflow Optimization to Reduce Time to Endovascular Reperfusion for Ultra-fast Stroke Treatment)

Clinical Trial Summary

The WE-TRUST study is a multi-center randomized clinical trial to assess the impact of a Direct to Angio Suite (DTAS) workflow on stroke patient outcomes.

Clinical Trial Description

Outcomes for stroke patients are closely tied to how fast they receive treatment. Currently, when a possible stroke patient arrives at the emergency department, typically first a CT or MRI exam is acquired for stroke triage. In case of an ischemic stroke the patient is then treated in an interventional suite. In the DTAS workflow stroke patients are diagnosed and treated in the interventional suite without interruption. The Cone-Beam CT (CBCT) capabilities of the interventional X-ray system are utilized to perform triage, directly followed by stroke treatment. The primary objective of the WE-TRUST study is to demonstrate that the DTAS triage workflow involving CBCT results in superior patient outcome in ischemic stroke patients with confirmed Large Vessel Occlusion as compared to the conventional CT/MR triage workflow. The WE-TRUST study will be running in 16 sites to enroll 500+ patients globally. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04701684
Study type Interventional
Source Philips Clinical & Medical Affairs Global
Contact Gerrits
Phone +31 6 55 48 29 31
Email carin.gerrits@philips.com
Status Recruiting
Phase N/A
Start date June 23, 2021
Completion date December 1, 2024
View Details
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