Mobilisation After Endovascular Stroke Treatment
Condition(s) studied
Investigational drug(s) / intervention(s)
Mobilisation: Out of bed mobilisation, such as sitting on the edge of the bed, standing or walking with or without support.
Study summary
The goal of this observational study is to learn how the timing of mobilisation after endovascular thrombectomy (EVT) affects complications in patients with acute ischaemic stroke. The main questions it aims to answer are:
Does mobilisation approximately 12 hours after EVT, compared to approximately 24 hours after EVT, affect the risk of complications such as access site haematoma (ASH), venous thromboembolism (VTE), infections, and delirium? How common are these complications after EVT, and which factors are associated with increased risk?
Participants undergoing EVT as part of their regular stroke care at two hospitals with different mobilisation routines will be followed during their hospital stay. Researchers will collect information about mobilisation timing, complications, clinical assessments, and medical history using case report forms, electronic health records, and national stroke registries.
Eligibility
Primary outcome measure(s)
- Access site haematoma — From completion of endovascular thrombectomy (baseline) to discharge from the stroke unit, up to 5 days.
Bleeding from puncture site
Trial sites (2)
| Facility | City | Region | Status |
|---|---|---|---|
| TAYS Tampere University Hospital | Tampere | Finland | Recruiting |
| Karolinska Institutet | Stockholm | Sweden | Recruiting |
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Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT07860333 on ClinicalTrials.gov ↗ ← All trials in Sweden