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NCT06975696Recruiting

Fusion Imaging in Endovascular Thrombectomy for Acute Ischemic Stroke

Source: ClinicalTrials.gov · Last updated 4 Mar 2026

Brief summary (registry, in English)

Endovascular thrombectomy (EVT) is the standard of care for acute ischemic stroke (AIS) caused by a large vessel occlusion. Successful recanalization is one of the most important factors for a good patient outcome, especially when obtained within 30 minutes from groin puncture, and the procedural success-rate reaches above 90% at treating centers of excellence. There are however a portion of cases where recanalization is not achieved, which in some cases are attributed to difficult arterial anatomy affecting the ability to catheterize the precerebral target vessel. In the latest angiography platforms, 3D reconstructions of the aortic, cervical and intracranial arteries from the preprocedural CT angiography can be fused with periprocedural 2D digital subtraction angiography and/or fluoroscopy images, so called 2D/3D Fusion imaging. The preparation steps can be done before patient arrival to the angiography suite and the image fusion can be done in less than a minute during patient preparation. Previous observational studies have shown that the use of fusion imaging during EVT procedures may decrease failed target vessel access and increase procedural success rate and first-pass recanalization rate, without prolonging the procedure. The purpose of this study is to assess the use of fusion imaging in EVT procedures and its effect on target vessel access, recanalization success-rate and procedure times.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
300 (estimated)
First submitted
28 Apr 2025
Start date
2 Mar 2026
Primary completion date
31 May 2027
Lead sponsor
Region Skane
Diseases
Stroke
NCT number
NCT06975696

What you commit to

  • Study type: Interventional
  • Planned participants: 300
  • From 2 Mar 2026 to the primary completion date, 31 May 2027
  • 4 sites in 2 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Previous inclusion in this study

Other

  • No access to a preoperative CTA

Who the study is looking for

  • Age ≥18 years.
  • Eligible for an EVT procedure

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (4)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Helsinki University Central Hospital
Coordinator of this site? Confirm its status
HelsinkiFinlandNot yet recruiting
Turku University Hospital
Coordinator of this site? Confirm its status
TurkuFinlandNot yet recruiting
Skåne University Hospital Lund
Coordinator of this site? Confirm its status
LundSwedenRecruiting
Örebro University Hospital
Coordinator of this site? Confirm its status
ÖrebroSwedenNot yet recruiting

This page is information, not medical advice. Discuss any trial with your doctor.