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
Sites (4)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Helsinki University Central Hospital Coordinator of this site? Confirm its status | Helsinki | Finland | Not yet recruiting |
| Turku University Hospital Coordinator of this site? Confirm its status | Turku | Finland | Not yet recruiting |
| Skåne University Hospital Lund Coordinator of this site? Confirm its status | Lund | Sweden | Recruiting |
| Örebro University Hospital Coordinator of this site? Confirm its status | Örebro | Sweden | Not yet recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.